Radial Artery Access Introducer Set CLI-422-07
Listed
Valid until
Not applicable
FDA recalls
1 ongoingDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00841268104082 | Date23 Feb 2018 | StatusListed |
Recalls
-
- Ongoing Z-1733-2025
Due to a potential open seal in the sterile barrier packaging .
-
- Terminated Z-2562-2018
- Terminated Z-2558-2018
The products listed might contain unsafe levels of bacterial endotoxins (Pyrogens) that were introduced during a manufacturing step. Bacterial Endotoxins also called pyrogenic bacteria can activate the inflammatory process and produce fever, chills, and hypotension in a patient.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- Radial Artery Access Introducer Set
- Generic Name
- Haemostasis valve
- Model / Ref / Catalog
- CLI-422-07
- Primary DI / UDI-DI
- 00841268104082
- FDA Product Code
- DYB
- GMDN Term
- Haemostasis valve
- Device Class
- Class II
- Regulation Number
- 870.1340
- GUDID distribution status
- Not in Commercial Distribution
- Sterilization Method
- Ethylene Oxide
- Size
- Catheter Gauge — 7 French
Other devices from Galt Medical Corp.
Properties
Other properties (8)
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Manufacturing Date: No