Identity
- Trade Name
- MAQUET CARDIOHELP FDA UDI
- Generic Name
- Cardiopulmonary bypass system, roller type FDA UDI
- Device Name
- CARDIOHELP Country Kit EnglUS FDA UDI
- Model / Reference
- CARDIOHELP Country Kit EnglUS FDA UDI
- Description
- CARDIOHELP Country Kit EnglUS FDA UDI
Identifiers
- Catalog Number
- 70105.2902 FDA UDI
- Primary DI / UDI-DI
- 04037691734941 FDA UDI
- 510(k) Number
- K133598 FDA UDI
- FDA Product Code
- DTQ FDA UDI
- GMDN Term
- Cardiopulmonary bypass system, roller type FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4220 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
Yes
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
Yes
FDA UDI
Maquet Cardiohelp by Maquet Cardiopulmonary AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K133598 also covers:
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
- Maquet Cardiopulmonary AG
Sources (1)
- FDA UDI 9b131830-1606-4550-a582-56d2a7d54bf1 37 fields · synced May 30, 2026