Identity
- Trade Name
- Bausch + Lomb FDA UDI
- Generic Name
- Corneal trephine, single-use FDA UDI
- Device Name
- Trephine Blade FDA UDI
- Model / Reference
- E3096 7.50 FDA UDI
- Description
- Trephine Blade FDA UDI
Identifiers
- Catalog Number
- E3096 7.50 FDA UDI
- Primary DI / UDI-DI
- 10757770055637 FDA UDI
- FDA Product Code
- HRH FDA UDI
- GMDN Term
- Corneal trephine, single-use 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
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
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Corneal trephine, single-use
Bausch + Lomb by Bausch & Lomb Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- coronet — Network Medical Products, Ltd. · Class I
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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
- Bausch & Lomb Incorporated
Sources (1)
- FDA UDI bbb88ae7-bb7a-4a09-87c0-8e77a4c0234b 34 fields · synced Jun 8, 2026