EX2721, TM220
by Eizo Corporation 2 variants
Part of a family of 175 devices: see the family page
Ref EX2721EDZZKS
EX2721, TM220 (EX2721-KS) is a Class I device made by Eizo Corporation, registered in EUDAMED on 18 Jun 2026 (Basic UDI-DI 4995047MonitorEndoscopeG5) and listed in FDA GUDID since 3 Jul 2018 (UDI-DI 04995047053118), active as of 24 Oct 2026.
Active
CE MDR
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/MDR EUDAMED | Number4995047MonitorEndoscopeG5 04995047053118 | Date18 Jun 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04995047053118 | Date3 Jul 2018 | StatusListed |
Official records
- EUDAMED public site 4995047MonitorEndoscopeG5
- AccessGUDID record 04995047053118
Across registries
- EUDAMED Basic UDI-DI 4995047MonitorEndoscopeG5 registered 18 Jun 2026 Active
- FDA GUDID UDI-DI 04995047053118 listed 3 Jul 2018 Listed
Timeline
- Listed FDA GUDID 04995047053118
- Registered EUDAMED 4995047MonitorEndoscopeG5
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- EX2721-Ks
- Generic name
- Endoscopic video image display unit
- Device name
- Endoscopic Monitor
- Model / Ref / Catalog
- EX2721EDZZKS EUDAMEDEX2721 GUDIDTM220 GUDIDEX2721-KS GUDID
- Primary DI / UDI-DI
- 04995047053118
- Basic UDI-DI
- 4995047MonitorEndoscopeG5
- FDA product code
- KQM
- EMDN code
- Z11900802 Bioimaging viewing monitors
- GMDN term
- Endoscopic video image display unit
- Device class
- Class I
- Regulation number
- 878.4160
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | EX2721EDZZKS | EX2721, TM220 |
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