Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Device sterilization/disinfection container, reusable FDA UDI
- Device Name
- V. Mueller DEEP INSTRUMENT CASSETTE WITH SILICONE MAT 8.0 X 4.5 X 1.2" 20.3 X 11.4 X 3.0 CM FDA UDI
- Model / Reference
- GP7-1250 FDA UDI
- Description
- V. Mueller DEEP INSTRUMENT CASSETTE WITH SILICONE MAT 8.0 X 4.5 X 1.2" 20.3 X 11.4 X 3.0 CM FDA UDI
Identifiers
- Catalog Number
- GP7-1250 FDA UDI
- Primary DI / UDI-DI
- 10885403047916 FDA UDI
- FDA Product Code
- KCT FDA UDI
- GMDN Term
- Device sterilization/disinfection container, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6850 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
No
FDA UDI
Over-the-Counter
Yes
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 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Carefusion 2200, Inc.
Sources (1)
- FDA UDI 5fce7eb6-84fd-40f4-a353-a0a122251beb 36 fields · synced Sep 18, 2026