MicroFrance® MCO2
Ref MCO2
MicroFrance® MCO2 is a Class I device made by Integra Microfrance, registered in EUDAMED on 1 Oct 2026 (Basic UDI-DI B-10381780107705) and listed in FDA GUDID since 12 Jan 2018 (UDI-DI 10381780107705), active as of 24 Oct 2026.
Active
CE MDD
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-10381780107705 10381780107705 | Date1 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number10381780107705 | Date12 Jan 2018 | StatusListed |
Official records
- EUDAMED public site B-10381780107705
- AccessGUDID record 10381780107705
Across registries
- EUDAMED Basic UDI-DI B-10381780107705 registered 1 Oct 2026 Active
- FDA GUDID UDI-DI 10381780107705 listed 12 Jan 2018 Listed
Timeline
- Listed FDA GUDID 10381780107705
- Registered EUDAMED B-10381780107705
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- MicroFrance®
- Generic name
- Middle ear chisel
- Device name
- ENT Manual Instruments
- Model / Ref / Catalog
- MCO2
- Primary DI / UDI-DI
- 10381780107705
- Basic UDI-DI
- B-10381780107705
- FDA product code
- JYE
- EMDN code
- L14050199, L140602
- GMDN term
- Middle ear chisel
- Device class
- Class I
- Regulation number
- 874.4420
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Belgium
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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