Medex MX7507
Medex MX7507 is a Class II device made by ICU Medical, Inc., listed in FDA GUDID since 29 Dec 2016 (UDI-DI 10351688505385), 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 | Number10351688505385 | Date29 Dec 2016 | StatusListed |
Official records
- AccessGUDID record 10351688505385
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Medex
- Generic name
- Tube/mask breathing circuit connector, single-use, sterile
- Model / reference
- MX7507
- Primary DI / UDI-DI
- 10351688505385
- 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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