Identity
- Trade Name
- MCV Infant ECC Pack with QPiD FDA UDI
- Generic Name
- Cardiopulmonary bypass system, non-roller type FDA UDI
- Device Name
- 701050970 BEQ-HMOD 30000-USA Pediatric Quadrox iD 701066544 BO-VHK 310000 Venous res Pediatric 701054444 Better Bladder 701020489 BEQ-RF32 RotaFLow 701045763 Gas Filter FDA UDI
- Model / Reference
- BEQ-TOP 28901 FDA UDI
- Description
- 701050970 BEQ-HMOD 30000-USA Pediatric Quadrox iD 701066544 BO-VHK 310000 Venous res Pediatric 701054444 Better Bladder 701020489 BEQ-RF32 RotaFLow 701045763 Gas Filter FDA UDI
Identifiers
- Catalog Number
- 701056771 FDA UDI
- Primary DI / UDI-DI
- 00607567205482 FDA UDI
- FDA Product Code
- DWE FDA UDI
- GMDN Term
- Cardiopulmonary bypass system, non-roller type FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4390 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Ethylene Oxide FDA UDI
MCV Infant ECC Pack with QPiD by Datascope Corp. — 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
- Datascope Corp.
Sources (1)
- FDA UDI ea3752b6-88ec-465c-a3ff-041c69e74131 37 fields · synced May 30, 2026