FDA Registration & Certification
About JJR Laboratory:
We provide professional FDA Approval services (including FDA 510K registration and FDA listing ) with competitive price that will help get your products to market faster, enabling greater sales and revenue. For technical regulation support, technicians at JJR are able to help you understand technical regulations and product design specifications. Communicate with our experts to determine your needs and we will provide you with a free evaluation, proposal and quotation.
Product We Test ： 1. Medical Devices 2. IVD (in vitro diagnostics) 3. Radiation-Emitting Products 4. Cosmetics 5.Animal Feed | Service We Supply: 1. Testing 2. Risk evaluation 3. Clinical evaluation 4. Technical documents 5. ISO 13485 |
What is FDA Approval ?
All the food, cosmetics, drugs, biological agents, medical equipment, and radio logical products must be FDA Approved before produced or imported in the United States.
Why Choose Us?
JJR Lab, accredited by CNAS, CMA, CNCA & A2LA, consistently operates competently and generates accurate and valid results in accordance with ISO/IEC 17025. We are also IECEE CB Scheme Test Laboratory (CBTL). Thus, testing reports from JJR Lab can be accepted between countries.
Your Benefits at a Glance:
1.20 Years of experience
JJR has extensive experience in all types of devices and regulatory requirements across markets.
2.Provide free modification service
Together with our wealth of knowledge in complex regulations globally, JJR provides a complete suite of testing solutions according to your needs including free modification service.
3.Save time to global markets
With over 7,000 square meters of labs, JJR offers the best testing cycles and you don't have to wait in line, JJR offers 1-on-1 service.With our in-depth insight of global product quality and regulatory requirements, JJR can optimize your costs and minimize your time to market.
4.Complete qualifications
ISO/IEC 17025 lab, accreditated by CNAS, CMA,A2LA,GLP.
5.Competitve price
Testing costs are lower than other labs.
Email:
hello@jjrlab.com
You can also contact us directly by email.
Test items and standards (active medical device):
Test items/products category | Standards ( CNAS accredited) |
General standards | |
EMC | IEC/EN60601-1-2， IEC/EN61326-1(-2-6)，FCC Part15/Part18， |
YY 9706.102， YY0505，GB/T18268.1，GB/T18268.26 | |
Safety | IEC/EN/ES60601-1，IEC/EN 60601-1-6(-1-8) (-1-9) (-1-11) (-1-12)， IEC/EN61010-1(-2-101)， |
GB9706.1-2020，YY/T9706.106，YY 9706.108， YY 9706.111，GB9706.112， | |
GB9706.1-2007，GB9706.15，YY0709，GB4793.1，YY/T0466.1 | |
Environment | GB/T14710 |
Special standards | |
Endoscope series | IEC/EN 60601-2-18，ISO8600系列， |
GB9706.218，GB9706.19，YY/T1603，YY/T0940，GB11244， YY/T1587，YY/T1603，YY1298，YY/T0763， YY/T0619，YY91083，YY0863，YY0864，YY/T0842， | |
YY1075，YY1082，YY/T0070，YY/T0071，YY/T0283， YY/T1028，YY0499，YY/T0189，YY0068系列 | |
Ultrasound series | IEC/EN60601-2-5(-2-37) (-2-62) (UD2/3)，IEC 62359，IEC61847， |
(diagnosis, physiotherapy) | GB 9706.205，GB9706.237，YY9706.262，GB 9706.7， GB9706.9，GB10152，YY/T0644，YY 0448，YY/T 1142， YY/T 1476，YY0906，GB/T16846，GB/T15214， YY/T1767，YY/T1090，YY/T0593，YY0767 |
Optical series | IEC/EN60601-2-22(-2-25) (-2-47) (-2-57) (-2-83)， IEC/EN60825，IEC/EN62471， |
GB 9706.222，YY 9706.257，GB9706.20，GB 7247.1， GB/T 20145，YY/T1496，YY0306，YY0323 | |
Monitoring equipment and accessories (blood oxygen, blood pressure, body temperature, ECG, etc.) | IEC/EN60601-2-27(-2-30) (-2-34) (-2-49)，ISO/EN80601-2-56(-2-59) (-2-61)， ISO81060，ASTM E1965， E1112， ANSI/AAMI EC53， |
GB9706.225，GB9706.227，YY 9706.234， YY 9706.247， YY 9706.249，YY0668，GB9706.27， YY1079，YY 0785，YY0667，YY 0670，YY/T 0783， YY 0784，GB/T21416，GB/T21417， YY 0828，YY 0601，YY/T0449，GB10793，YY1139， YY0782，YY0828，YY/T 0196，YY/T 0885 | |
Nerve and Muscle Stimulators | IEC/EN60601-2-10， |
YY 9706.210，YY0607，YY0896，YY1095，YY/T0696，YY0868 | |
High frequency class and accessories | IEC/EN60601-2-2， |
GB9706.202，GB9706.4，YY 0601，YY0322 | |
Infusion pump/syringe pump | IEC/EN60601-2-24， |
GB9706.224，GB9706.27 | |
Oral | IEC/EN60601-2-60，ISO7785.1， |
GB9706.260，YY1045，YY0059，YY0836， YY0837，YY/T1485，YY/T1147，YY/T1400， YY/T1401，YY/T1602，YY/T1684，YY/T1120，YY/T1692， YY0460，YY0055，YY/T1043，YY/T0058，YY0059 | |
Hospital beds, operating tables | IEC/EN 60601-2-46(-2-52), |
YY 9706.246，YY 9706.252，YY0570，YY0571，YY/T1106 | |
Oxygen production equipment | EN/ISO 80601-2-69， |
YY 9706.269，YY/T 0298 | |
In vitro diagnostics IVD | IEC/EN61010-2-010(-2-020) (-2-030) (-2-040) (-2-051) (-2-081)，ISO15197 |
YY 0648，GB 4793.3，GB 4793.6，GB 4793.7，GB 4793.9，GB/T19634， | |
Test items and standards (non-active medical device):
Test items/products category | Standards ( CNAS accredited) | |
Biocompatibility | ||
Physical and / or chemical information | ISO 10993-18、GB/T 16886.18 | |
Evaluation and testing within a risk management process | ISO 10993-1、GB/T 16886.1 | |
Genotoxicity (Ames, chromosomal aberrations, genetic mutations, micronuclei) | ISO 10993-3、GB/T 16886.3 | |
Hemolysis (rabbit blood), platelet count, complement activation, in vivo thrombosis, coagulation(PTT,PT) | ISO 10993-4、GB/T 16886.4 | |
ASTM Hemolysis (rabbit blood, human blood) | ASTM F 756-17 | |
Cytotoxicity (MTT method, direct contact method, microscope observation method, agar method, membrane filtration method) | ISO10993-5、GB/T 16886.5 | |
Implantation (muscle, subcutaneous, bone) | ISO 10993-6、GB/T 16886.6 | |
EO Residue | ISO10993-7、GB/T 16886.7 | |
Sensitization (direct contact method, occlusive application) | ISO 10993-10、GB/T 16886.10、GB15979 | |
Irritation (dermal, multiple dermal, intradermal, oral, ocular, penis, vaginal, rectal, direct contact, occlusive patches) | ISO 10993-10、GB/T 16886.10 | |
Acute toxicity, pyrogen, chronic toxicity, carcinogenic | ISO 10993-11、GB/T 16886.11 | |
Subacute systemic toxicity (oral, intravenous, intraperitoneal, subcutaneous implantation) | ISO 10993-11、GB/T 16886.11 | |
Subchronic systemic toxicity (oral, intravenous, intraperitoneal, subcutaneous implant, intramuscular implant, bone implant) | ISO 10993-11、GB/T 16886.11 | |
immunogenic | ISO10993-20、GB/T16886.20 | |
In vitro irritation test | ISO10993-23 | |
USP Class 6 Biocompatible | USP87、USP88 | |
Cleaning, Disinfection, Sterilization Validation | ||
Cleaning, Disinfection, Sterilization Validation | AAMI TIR30、AAMI TIR12、ASTM 3208-20、WS 310、WS/T 367、YY/T 0734、ISO 20857、ISO 25424、ISO 17664、ISO 17665 | |
Packaging Verification | ||
Simulate transport | ISTA 2A/3A、ASTM D4169 | |
Packaging Verification: Accelerated aging, vacuum leak, dye leak, seal peel, agar attack, sterility, visual, burst, air bubbles | ASTM F 1980-16、ASTM D3078-02、ASTM F1929、ASTM F88-15、DIN 58953-6-2016、USP、ISO11737-2、ASTM F1886、ASTM F1140、ASTM F 2096-11、YY/T 0681.1、GB15171、YY/T 0681.4、YY/T 0681.2、CP、GB14233.2、YY/T 0681.11、YY/T 0681.3、YY/T 0681.14、、YY/T 0681.5 | |
Test items and standards (Chemical and physical performance):
Chemical performance | Standards/Items |
Chemical Analysis and EO Residues | Turbidity, color, reducing substances, chloride, pH, evaporation residue, UV absorbance, residue on ignition, heavy metals, EO residue, ECH 2-chloroethanol residue, ETG ethylene glycol residue, collagen content, viscosity |
breathing circuit | ISO 18562-1、ISO 18562-2、ISO 18562-3、ISO 18562-4 |
Physical performance | Standards/Items |
Interventional devices (catheters); Medical excipients; Medical surgical instruments | Size, Surface Roughness, Flexibility, Breaking Force, Resistance to Bending Damage, Radiodetectability, Corrosion Resistance, Peak Tensile Force, Joint Firmness, Toughness, Tensile, Hardness, Compressive Strength, Burst Test, Heat Resistance, Leakage, particle contamination, gravity bearing, conical joints, flattening resistance, bending resistance, sliding performance, tightness, transparency, fit, patency, elasticity, rigidity... |
Test items and standards (microorganism):
microorganism | Standards/Items |
Microorganisms (bioburden, microbial limit, total bacteria, initial contaminating bacteria, bacteriostatic effect, sterility) | ISO11737-1、ISO11737-2、CP、GB14233.2、USP、GB15979、GB19083、GB/T 19973.1、GB/T 19973.2、ISO 11137-1、ISO11137-2、GB18280.1、GB18280.2 |
Bacterial endotoxin (gel limit method, quantitative chromogenic matrix method) | CP，USP，EP |
Test Procedure:
1. Provide us with product pictures, product brochures/manuals
2. Determine your needs（test report purpose/ test itmes/ standards）
3. Receive the testing/compliance service proposal and quotation
4. Sign contract and make payment
5.Send samples (please contact us for address info.)
6.Informed project opening and test TAT(turn around time) via email
7.Testing
8.Draft report for your confirmation
9. Formal reports endorsed by ILAC - CNAS (electronic version)
10.Sample Discard or Return
FDA supervise requirements:
FDA has established classifications for approximately 1,700 different types of devices, grouping them into 16 broad medical classes. All these are divided into three risk levels , class I, class II ,class III.
CLASS I | CLASS II | CLASS III |
Listing / 510(k) (few) | 510 (k) / PMA(few) | PMA |
Clinical research Products R&D Plan PMA | ||
Performance Post-market surveillance Efficacy feedback registration | special label requirements Premarket Data Requirements Guidance | |
Enterprise registration Products Listing Inappropriate labeling
| 510k 21 CFR 820 GMP/QSR Records and testing reports | |
Sample Requirements:
Pls prepare the samples after our verification.
The samples should be provided safely with standard shipping status. Please provide the samples with sterile barrier packaging if the product is planned to sell under sterile conditions. Have a question about product testing and certification? If possible, kindly tell us ‘how did you hear about us’.
Email us at hello@jjrlab.com.
JJR Service procedure for FDA registration:
Test items and standards (wireless medical device):
Wireless Medical device and IVD | ||||||
RF Test | (USA) FCC ID | (Canada) IC | (EU) CE-RED | (UK) UKCA | (China) SRRC | (AU) RCM |
NFC RFID-13.56MHz | FCC Part15.225 | RSS-210 | EN300 330 | EN300 330 | exempted | AN/NZS 4268 |
Bluetooth WIFI - 2.4G | FCC Part15.247 | RSS-247 | EN300 328 | EN300 328 | 信部无[2002]353号 | AN/NZS 4268 |
WIFI - 5G | FCC Part15.407 | RSS-247 | EN301 893 | EN301 893 | 工信部无函[2012]620号, | AN/NZS 4268 |
WCDMA LTE | FCC Part22, 24, 27 | RSS-132/133/139 | EN301 908-2/-13 | EN301 908-2/-13 | 工信部无函[2015]135号, | AS/CA S042.1 |
Wireless coexistence test | ANSI C63.27, AAMI TIR69 | |||||
Animal consumption (including pet food) FDA registration
As required by the FDA Food, Drug, and Cosmetic Act：
All Animal consumption (including pet food), like human food, must be produced under sanitary conditions, free of harmful substances, and truthfully labeled to ensure safe.
For additives in Animal consumption (including pet food), feed additives must be approved according to 21 CFR 570, 571, and 573. in the case of food additives that are not on the list in 21 CFR 573 or on the list but have a new intended use require a FAP application.
Colorants must be approved as specified in 21 CFR 70 and listed in Part 73, 74, or 81.
Animal consumption (including pet food) FDA registration classification：
Oilseed or Oilseed Products Grain or Grain Products Alfalfa Products or Lespedeza Products; Amino Acids or Related Products; Animal Protein Products* Botanicals and Herbs*; Brewer Products; Chemical Preservatives; Citrus Products;
| Distillery Products; Direct Fed Microbials*; Enzymes; Fats or Oils; Fermentation Products; Forage Products*; Human food by-products not otherwise listed*; Marine Products; Milk Products; Minerals or Mineral Products; Miscellaneous or Special Purpose Products; Molasses or Molasses Products; Non-protein Nitrogen Products;
| Peanut Products; Processed Animal Waste Products* Screenings; Technical Additives*; Vitamins or Vitamin Products; Yeast Products; Mixed Feed Pet Food; Pet Treats or Pet Chews; Pet Nutritional Supplements Pet Nutritional Supplements
|
Animal consumption (including pet food) FDA labeling requirements
1, FDA regulation
Federal regulations labeling requirements include Animal consumption net content table (weight, volume, or quantity), the name and address of the manufacturing, packaging, and distribution company, listing the content of different ingredients in the product in descending order, listing common or generic product names.
2, Other requirements
Some states also enforce their own labeling regulations, and most pet foods follow the Association of American Feed Control Officials (AAFCO) for pet food management.
CCIC-JJR FDA registration tips:
1. Animal consumption (including pet food) FDA registration, how long is it valid?
Valid for 2 years, then need to renew the registration every 2 years.
2. Do multiple products need FDA registration separately?
No. FDA registration for Animal consumption is done by enterprise according to product categories.
3. Will a certificate be provided after FDA registration?
There is no certification, we will provide the enterprise FDA registration number and PIN code.
Registration Number: The registration number given to the company by FDA;
PIN: The personal identification number of the registered company.
4. How long it will take to finish FDA registration for Animal consumption (including pet food)?
Depending on the FDA response time, generally no more than 1 weeks.
5. Do I need a U.S. agent?
Yes, if the company does not have a U.S. agent, we can provide agent services.
6. What do the labels contain?
l The name of the product.
l The species of animals for which the product is intended.
l A description of the amount of food in the package or container.
l A list of all ingredients in the product.
l A statement of nutritional adequacy, if required.
l The name and address of the manufacturer or distributor.
