Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Spinal rongeur FDA UDI
- Device Name
- MICRO HANDLE TAKE APART KERRISON RONGEUR, NON-COATED 40DEG UP, 5MM BITE, 10MM OPENING SHAFT LENGTH 10" (25.4CM) FDA UDI
- Model / Reference
- NL4291-05 FDA UDI
- Description
- MICRO HANDLE TAKE APART KERRISON RONGEUR, NON-COATED 40DEG UP, 5MM BITE, 10MM OPENING SHAFT LENGTH 10" (25.4CM) FDA UDI
Identifiers
- Catalog Number
- NL4291-05 FDA UDI
- Primary DI / UDI-DI
- 10885403187995 FDA UDI
- FDA Product Code
- HAE FDA UDI
- GMDN Term
- Spinal 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 6733c16b-a99c-45e8-aa2e-221d240a8082 36 fields · synced Sep 18, 2026