Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Cardiopulmonary bypass cannula, femoral FDA UDI
- Device Name
- V. Mueller MAYO ILIAC-FEMORAL CANNULA 3MM I.D. FDA UDI
- Model / Reference
- CH8000-019 FDA UDI
- Description
- V. Mueller MAYO ILIAC-FEMORAL CANNULA 3MM I.D. FDA UDI
Identifiers
- Catalog Number
- CH8000-019 FDA UDI
- Primary DI / UDI-DI
- 10885403033681 FDA UDI
- FDA Product Code
- DWF FDA UDI
- GMDN Term
- Cardiopulmonary bypass cannula, femoral FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4210 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 a85b502b-808f-42f1-8f31-6df5b442a10e 36 fields · synced Sep 18, 2026