Temena 31950-21
by Temena GmbH
Temena 31950-21 is a Class II device made by Temena GmbH, listed in FDA GUDID since 28 Nov 2017 (UDI-DI 03700339713523), 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 | Number03700339713523 | Date28 Nov 2017 | StatusListed |
Official records
- AccessGUDID record 03700339713523
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Temena
- Generic name
- Spinal needle, single-use
- Model / Ref / Catalog
- 31950-21
- Primary DI / UDI-DI
- 03700339713523
- FDA product code
- BSP
- GMDN term
- Spinal needle, single-use
- Device class
- Class II
- Regulation number
- 868.5150
- GUDID distribution status
- In Commercial Distribution
- Size
- Needle Gauge — 21 GaugeLength — 123 Millimeter
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