Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Cervical anaesthesia needle, reusable FDA UDI
- Device Name
- PUDENDAL AND PARASYMPATHETIC BLOCK ANESTHESIA NEEDLE 20GA OVERALL LENGTH 6 inches15.2CM FDA UDI
- Model / Reference
- HY21319 FDA UDI
- Description
- PUDENDAL AND PARASYMPATHETIC BLOCK ANESTHESIA NEEDLE 20GA OVERALL LENGTH 6 inches15.2CM FDA UDI
Identifiers
- Catalog Number
- HY21319 FDA UDI
- Primary DI / UDI-DI
- 10885403051739 FDA UDI
- FDA Product Code
- FMI FDA UDI
- GMDN Term
- Cervical anaesthesia needle, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5570 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
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
Category: Cervical anaesthesia needle, reusable
V. Mueller by Steris Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cervical anaesthesia needle, reusable.
- V. Mueller — STERIS CORPORATION · Class II
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
- Steris Corporation
Sources (1)
- FDA UDI 82ab396b-609b-485b-b04f-edac8c4779ab 35 fields · synced Jun 8, 2026