Chkd 3/8” Ecc Beq-Top 31603
Chkd 3/8” Ecc Beq-Top 31603 (709000516) is a Class II device made by Datascope Corp., listed in FDA GUDID since 24 Jul 2018 (UDI-DI 00607567212510), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00607567212510 | Date24 Jul 2018 | StatusListed |
Official records
- AccessGUDID record 00607567212510
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Chkd 3/8” Ecc
- Generic name
- Cardiopulmonary bypass system blood tubing set
- Model / Ref / Catalog
- BEQ-TOP 31603, 709000516
- Primary DI / UDI-DI
- 00607567212510
- FDA product code
- DWE
- GMDN term
- Cardiopulmonary bypass system blood tubing set
- Device class
- Class II
- Regulation number
- 870.4390
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Ethylene Oxide
Similar devices
Other devices filed under FDA product code DWE (Tubing, Pump, Cardiopulmonary Bypass).
- Extracorp.'s Intersept CUS Tubing PK by Extracorporeal Medical Specialities, Inc.
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- CHEST DRAINAGE TUBING by Olson Medical Sales, Inc.
- CARDIOPULMONARY BYPASS PUMP TUBING by Texas Medical Products, Inc.
- HLM TUBING SET WITH BIOLINE COATING by Maquet Cardiopulmonary AG
- PUMP TUBING WITH X-COATING by Terumo Cardiovascular Systems Corporation
- GENTLE HEADER by Enhanced Perfusion Systems, Inc.
- Terumo Pump Tubing by Terumo Cardiovascular Systems Corporation
- TYGON TUBING by Electromedics, Inc.