Identity
- Trade Name
- REACT FDA UDI
- Generic Name
- Instrument tray, reusable FDA UDI
- Device Name
- 3.5MM STERLING REACT, FULL RADIUS RESECTOR 6 EA FDA UDI
- Model / Reference
- 35FRR-RA-ZZ FDA UDI
- Description
- 3.5MM STERLING REACT, FULL RADIUS RESECTOR 6 EA FDA UDI
Identifiers
- Catalog Number
- 35FRR-RA-ZZ FDA UDI
- Primary DI / UDI-DI
- 10845854029404 FDA UDI
- FDA Product Code
- GFA FDA UDI
- GMDN Term
- Instrument tray, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4820 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 3.5 Millimeter FDA UDI
React by Conmed Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Conmed Corporation
Sources (1)
- FDA UDI c2a64e87-57ba-42bd-b29c-c73d4c008a49 38 fields · synced Jun 1, 2026