Portex 6947-02
Portex 6947-02 is a Class II device made by ICU Medical, Inc., listed in FDA GUDID since 13 Dec 2016 (UDI-DI 00351688056071), 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 | Number00351688056071 | Date13 Dec 2016 | StatusListed |
Official records
- AccessGUDID record 00351688056071
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Portex
- Generic name
- Epidural anaesthesia set, non-medicated
- Model / reference
- 6947-02
- Primary DI / UDI-DI
- 00351688056071
- FDA product code
- BSO
- GMDN term
- Epidural anaesthesia set, non-medicated
- Device class
- Class II
- Regulation number
- 868.5120
- GUDID distribution status
- In Commercial Distribution
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