Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Device sterilization/disinfection container, reusable FDA UDI
- Device Name
- V. Mueller MICROSURGICAL INSTRUMENT TRAY BASE LID & MAT 15X10X4/5" (38.1X25.4X2CM) FDA UDI
- Model / Reference
- SU2990-080 FDA UDI
- Description
- V. Mueller MICROSURGICAL INSTRUMENT TRAY BASE LID & MAT 15X10X4/5" (38.1X25.4X2CM) FDA UDI
Identifiers
- Catalog Number
- SU2990-080 FDA UDI
- Primary DI / UDI-DI
- 10885403131936 FDA UDI
- FDA Product Code
- FSM FDA UDI
- GMDN Term
- Device sterilization/disinfection container, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
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 76d20b8b-8937-41fb-9b3d-f2f8d134d61a 36 fields · synced Jun 6, 2026