Temena 09090-21
by Temena GmbH
Temena 09090-21 is a Class II device made by Temena GmbH, listed in FDA GUDID since 28 Nov 2017 (UDI-DI 03700339710669), registry data as of 12 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number03700339710669 | Date28 Nov 2017 | StatusListed |
Official records
- AccessGUDID record 03700339710669
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Temena
- Generic name
- Peripheral anaesthesia catheter set, non-medicated
- Model / Ref / Catalog
- 09090-21
- Primary DI / UDI-DI
- 03700339710669
- FDA product code
- CAZ
- GMDN term
- Peripheral anaesthesia catheter set, non-medicated
- Device class
- Class II
- Regulation number
- 868.5140
- GUDID distribution status
- In Commercial Distribution
- Size
- Needle Gauge — 21 GaugeLength — 101.3 Millimeter
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