Identity
- Trade Name
- 6ft x 1/4 x 1/16 Tubing FDA UDI
- Generic Name
- Cardiopulmonary bypass system blood tubing set FDA UDI
- Model / Reference
- BEQ- 20102 FDA UDI
Identifiers
- Catalog Number
- 701048429 FDA UDI
- Primary DI / UDI-DI
- 00607567200159 FDA UDI
- GMDN Term
- Cardiopulmonary bypass system blood tubing set FDA UDI
Classification
- 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
6ft x 1/4 x 1/16 Tubing by Datascope Corp. — 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 | N/A | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Datascope Corp.
Sources (1)
- FDA UDI e15ccbf7-fe43-4ba7-807f-bf1eafa3ec4e 36 fields · synced May 29, 2026