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,INSERT TRAY & 2 MATS 10X6X1-1/2" (25.4X15.2X3.8CM) FDA UDI
- Model / Reference
- SU2990-060 FDA UDI
- Description
- V. Mueller MICROSURGICAL INSTRUMENT TRAY BASE,LID,INSERT TRAY & 2 MATS 10X6X1-1/2" (25.4X15.2X3.8CM) FDA UDI
Identifiers
- Catalog Number
- SU2990-060 FDA UDI
- Primary DI / UDI-DI
- 10885403131929 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 520ebc68-fd2f-4cf1-8956-a65e02107b5b 36 fields · synced Sep 18, 2026