Arrow IPN045757
Arrow IPN045757 (ASK-20608-ROP) is a Class II device made by Teleflex Incorporated, listed in FDA GUDID since 16 Sep 2016 (UDI-DI 00801902063137), registry data as of 22 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 | Number00801902063137 | Date16 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00801902063137
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Arrow
- Generic name
- Peripheral anaesthesia single-administration set, non-medicated
- Model / Ref / Catalog
- IPN045757, ASK-20608-ROP
- Primary DI / UDI-DI
- 00801902063137
- FDA product code
- CAZ
- GMDN term
- Peripheral anaesthesia single-administration set, non-medicated
- Device class
- Class II
- Regulation number
- 868.5140
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 60 Centimeter
Similar devices
Other devices filed under FDA product code CAZ (Anesthesia conduction kit).
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- ECHOBRIGHT by Life-Tech Intl., Inc.
- EPISPIN, EPISPIN II SAFETY, EPISPIN II, EPISPIN I, EPISPIN IV by Pajunk GmbH