Identity
- Trade Name
- BR Surgical, LLC FDA UDI
- Generic Name
- Orbital depressor, reusable FDA UDI
- Device Name
- SCHOCKET scleral depressor w/ pocket clip, double-ended FDA UDI
- Model / Reference
- BR42-32814 FDA UDI
- Description
- SCHOCKET scleral depressor w/ pocket clip, double-ended FDA UDI
Identifiers
- Catalog Number
- BR42-32814 FDA UDI
- Primary DI / UDI-DI
- 00840183521998 FDA UDI
- FDA Product Code
- HNX FDA UDI
- GMDN Term
- Orbital depressor, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 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: Orbital depressor, reusable
BR Surgical, LLC by Br Surgical Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orbital depressor, reusable.
- Ambler Surgical — Ambler Surgical, LLC · Class I
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- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
- MILLENNIUM — AVALIGN TECHNOLOGIES, Inc. · Class I
- V. Mueller — STERIS CORPORATION · Class I
- Bausch + Lomb — Bausch & Lomb Incorporated · Class I
- Schepens Scleral Depressor — SONTEC INSTRUMENTS, INC. · Class I
- Ambler Surgical — Ambler Surgical, LLC · Class I
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 7bbc5bf1-371e-47e8-9f73-9a073a2e1a08 35 fields · synced May 30, 2026