Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Peripheral nerve-block sharp needle FDA UDI
- Device Name
- V. Mueller PARACERVICAL AND PUDENDAL NERVE BLOCK NEEDLE OVERALL LENGTH 8" (20.3CM) RETRACTED FDA UDI
- Model / Reference
- GL5150 FDA UDI
- Description
- V. Mueller PARACERVICAL AND PUDENDAL NERVE BLOCK NEEDLE OVERALL LENGTH 8" (20.3CM) RETRACTED FDA UDI
Identifiers
- Catalog Number
- GL5150 FDA UDI
- Primary DI / UDI-DI
- 10885403046742 FDA UDI
- FDA Product Code
- FMI FDA UDI
- GMDN Term
- Peripheral nerve-block sharp needle FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5570 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 II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Carefusion 2200, Inc
Sources (1)
- FDA UDI d2e2a81a-8830-4cef-89a3-2b9a555b192b 36 fields · synced Jun 6, 2026