Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
- Device Name
- V. Mueller AZAR UTILITY FORCEPS STRAIGHT TIPS SERRATED 3MM FROM END OVERALL LENGTH 4" (10.2CM) FDA UDI
- Model / Reference
- OP3295 FDA UDI
- Description
- V. Mueller AZAR UTILITY FORCEPS STRAIGHT TIPS SERRATED 3MM FROM END OVERALL LENGTH 4" (10.2CM) FDA UDI
Identifiers
- Catalog Number
- OP3295 FDA UDI
- Primary DI / UDI-DI
- 10885403098239 FDA UDI
- FDA Product Code
- HNR FDA UDI
- GMDN Term
- Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
V. Mueller by Carefusion 2200, Inc — 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 |
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Manufacturer
- Manufacturer
- Carefusion 2200, Inc
Sources (1)
- FDA UDI ad3e0150-3d0e-4f5e-84aa-a01b89f0a50f 36 fields · synced Jun 8, 2026