Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Orthopaedic joint/limb rongeur FDA UDI
- Device Name
- V. Mueller Neuro/Spine CHROMA-LINE SPINAL RONGEUR SINGLE RING HANDLE 4MM, STRAIGHT, TURQUOISE SHAFT LENGTH 9" (230MM) FDA UDI
- Model / Reference
- U-0735 FDA UDI
- Description
- V. Mueller Neuro/Spine CHROMA-LINE SPINAL RONGEUR SINGLE RING HANDLE 4MM, STRAIGHT, TURQUOISE SHAFT LENGTH 9" (230MM) FDA UDI
Identifiers
- Catalog Number
- U-0735 FDA UDI
- Primary DI / UDI-DI
- 10885403138645 FDA UDI
- FDA Product Code
- HAE FDA UDI
- GMDN Term
- Orthopaedic joint/limb rongeur FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4840 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 215d3c15-c767-41f9-af96-a52ff378dc7a 36 fields · synced Sep 18, 2026