Main Meditech
by Main MediTech Co., Ltd 32 variants
Ref SG-2000
Main Meditech (SG-2000) is a Class I device made by Main MediTech Co., Ltd, registered in EUDAMED on 4 Aug 2026 (Basic UDI-DI 697499888SLSG5Y), active as of 25 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number697499888SLSG5Y | Date4 Aug 2026 | StatusActive |
Official records
- EUDAMED public site 697499888SLSG5Y
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- Slit Lamp G SerieDry Eye Tester
- Model / reference
- SG-2000
- Primary DI / UDI-DI
- 06974998880231, 06974998880392
- Basic UDI-DI
- 697499888SLSG5Y, 697499888SGBF
- Direct marketing DI
- 0697499888023106974998880392
- EMDN code
- Q0299 Ophthalmic devices - other
- Device class
- Class I
- System or procedure pack
- Procedure pack which is a device in itself
- EU registration type
- Standard device
- EU market of registration
- Greece
Manufacturer details
- EUDAMED SRN
- CN-MF-000010962
- Authorised representative
- Umedwings Netherlands B.V. NL-AR-000000444
From the manufacturer
Manufacturer's product page: Website: www.mainmeditech.com
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