Medex MX20067
Medex MX20067 is a Class II device made by ICU Medical, Inc., cleared under FDA 510(k) K952160 on 21 Sep 1995 and listed in FDA GUDID since 11 Oct 2016 (UDI-DI 10351688509826), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10351688509826 | Date11 Oct 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK952160 | Date21 Sep 1995 | StatusActive |
Official records
- AccessGUDID record 10351688509826
- FDA 510(k) database K952160
Across registries
- FDA 510(k) K952160 decided 21 Sep 1995 Active
- FDA GUDID UDI-DI 10351688509826 listed 11 Oct 2016 Listed
Timeline
- Cleared FDA 510(k) K952160
- Listed FDA GUDID 10351688509826
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Medex
- Generic name
- Tube/mask breathing circuit connector, single-use, sterile
- Model / reference
- MX20067
- Primary DI / UDI-DI
- 10351688509826
- 510(k) Number
- FDA product code
- FPA
- GMDN term
- Tube/mask breathing circuit connector, single-use, sterile
- Device class
- Class II
- Regulation number
- 880.5440
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Ethylene Oxide
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