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Peet Laser Forceps for Laser (splinter forceps, S-shaped) (non glare)
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Peet Laser Forceps for Laser (splinter forceps, S-shaped) (non glare) FDA UDI
- Generic Name
- Clamp manipulation forceps FDA UDI
- Device Name
- Stainless Steel Forceps for Laser (splinter forceps, S-shaped) (non glare) FDA UDI
- Model / Reference
- 25-211 FDA UDI
- Description
- Stainless Steel Forceps for Laser (splinter forceps, S-shaped) (non glare) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10697660003532 FDA UDI
- FDA Product Code
- GEN FDA UDI
- GMDN Term
- Clamp manipulation forceps FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- Not 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
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 11.5 Centimeter FDA UDILength — 4.5 Inch FDA UDI
Peet Laser Forceps for Laser (splinter forceps, S-shaped) (non glare) by Oculo-Plastik Inc — Class I — FDA UDI — listed in FDA GUDID
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
- Oculo-Plastik Inc
Sources (1)
- FDA UDI 21251770-d358-4111-8029-b6bfa4a7a0ea 36 fields · synced May 30, 2026