Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Wire cutter FDA UDI
- Device Name
- V. Mueller VITAL ADVANCED REPLACEMENT TC INSERTS FOR OS3036 FDA UDI
- Model / Reference
- OS3036-001 FDA UDI
- Description
- V. Mueller VITAL ADVANCED REPLACEMENT TC INSERTS FOR OS3036 FDA UDI
Identifiers
- Catalog Number
- OS3036-001 FDA UDI
- Primary DI / UDI-DI
- 10885403102851 FDA UDI
- FDA Product Code
- HXZ FDA UDI
- GMDN Term
- Wire cutter FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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 0abaa63e-e7fb-43ec-844f-fa49b3e411a0 36 fields · synced Jun 8, 2026