Perfusion Adapter Set 301022NS
Perfusion Adapter Set 301022NS (331022NS) is a cardioplegia solution administration adaptor (FDA Class II; FDA product code DWF, Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass) made by Novosci Corp., listed in FDA GUDID since 9 Oct 2015 (UDI-DI B066301022NS1), 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 | NumberB066301022NS1 | Date9 Oct 2015 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Perfusion Adapter Set
- Generic name
- Cardioplegia solution administration adaptor
- Model / Ref / Catalog
- 301022NS, 331022NS
- Primary DI / UDI-DI
- B066301022NS1
- FDA product code
- DWF
- GMDN term
- Cardioplegia solution administration adaptor
- Device class
- Class II
- Regulation number
- 870.4210
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Ethylene Oxide
Similar devices
Other devices filed under FDA product code DWF (Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass).
- Quantum Perfusion Dual Lumen Cannula 31F-V1 (DL31F-V1) by Spectrum Medical S.R.L.
- Circuit Tubings with X-Coating by Terumo Cardiovascular Systems Corporation
- COBE HEART/LUNG PERFUSION AND CARDIOPLEGIA PACK by Cobe Laboratories, Inc.
- Vortex Cannula by Vortex Medical, Inc.
- Malleable Single Stage Venous Cannula with Carmeda Bioactive Surface, Model CB681XX Series by MEDTRONIC PERFUSION SYSTEMS
- Sundt™ NL8505079 by Integra Lifesciences Corp.
- Pediatric Arterial Cannula by Polystan A/S
- Sundt™ NL8505072 by Integra Lifesciences Corp.
- Cardiopulmonary Bypass by Dlp, Inc.
- Quantum Perfusion Dual Lumen Cannula 24F, 24F-V1, 27F, 27F-V1, 27F-VS, 29F, 29F-V1, 31F, 31F-VS by Qura S.R.L