Identity
- Trade Name
- VBT Venous Bubble Trap FDA UDI
- Generic Name
- Blood transfusion filter FDA UDI
- Device Name
- Venous Bubble Trap, BIOLINE Coating (BEQ), and sterile. The Venous Bubble Trap VBT 160 is designed to remove gross air in the venous line before it is entering the arterial pump and the following components of the extra corporeal circuit (ECC). The VBT has been especially developed as an additional safety feature for minimized systems, e.g. MECC, where venous reservoirs are missing. The VBT is using different physical principals for air removal. FDA UDI
- Model / Reference
- BEQ-VBT 160, BIOLINE, Sterile FDA UDI
- Description
- Venous Bubble Trap, BIOLINE Coating (BEQ), and sterile. The Venous Bubble Trap VBT 160 is designed to remove gross air in the venous line before it is entering the arterial pump and the following components of the extra corporeal circuit (ECC). The VBT has been especially developed as an additional safety feature for minimized systems, e.g. MECC, where venous reservoirs are missing. The VBT is using different physical principals for air removal. FDA UDI
Identifiers
- Catalog Number
- 70103.0884 FDA UDI
- Primary DI / UDI-DI
- 04037691075051 FDA UDI
- FDA Product Code
- DTP FDA UDI
- GMDN Term
- Blood transfusion filter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4230 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
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 160 Milliliter FDA UDI
VBT Venous Bubble Trap by Maquet Cardiopulmonary AG — 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
- Maquet Cardiopulmonary AG
Sources (1)
- FDA UDI e035d8d8-5df8-4a88-ab01-3d5ae8514276 37 fields · synced May 30, 2026