Arrow IPN925295
Arrow IPN925295 (ASK-04001-KB) is a Class II device made by Teleflex Incorporated, listed in FDA GUDID since 11 Jul 2022 (UDI-DI 10801902211528), 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 | Number10801902211528 | Date11 Jul 2022 | StatusListed |
Official records
- AccessGUDID record 10801902211528
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Arrow
- Generic name
- Epidural anaesthesia set, medicated
- Model / Ref / Catalog
- IPN925295, ASK-04001-KB
- Primary DI / UDI-DI
- 10801902211528
- FDA product code
- BSO
- GMDN term
- Epidural anaesthesia set, medicated
- Device class
- Class II
- Regulation number
- 868.5120
- GUDID distribution status
- In Commercial Distribution
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