Identity
- Trade Name
- BR Surgical, LLC FDA UDI
- Generic Name
- ENT soft-tissue cutting forceps FDA UDI
- Device Name
- MIDDLETON-JANSEN Septum Forceps, 3mm x 13mm thru cutting jaws, narrow shafts, 7 1/2" FDA UDI
- Model / Reference
- BR46-32518 FDA UDI
- Description
- MIDDLETON-JANSEN Septum Forceps, 3mm x 13mm thru cutting jaws, narrow shafts, 7 1/2" FDA UDI
Identifiers
- Catalog Number
- BR46-32518 FDA UDI
- Primary DI / UDI-DI
- 00840183515195 FDA UDI
- FDA Product Code
- KAE FDA UDI
- GMDN Term
- ENT soft-tissue cutting forceps FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4420 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: ENT soft-tissue cutting forceps
BR Surgical, LLC by Br Surgical Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 |
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Manufacturer
- Manufacturer
- Br Surgical Llc
Sources (1)
- FDA UDI 160f73c3-56e6-4586-9aa0-8c4f09301e32 35 fields · synced Jun 8, 2026