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Main Meditech

by Main MediTech Co., Ltd 32 variants

Ref HULK

Main Meditech (HULK) is a Class I device made by Main MediTech Co., Ltd, registered in EUDAMED on 4 Aug 2026 (Basic UDI-DI 697499888TableKH), active as of 25 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697499888TableKH Basic UDI-DI 06974998880361UDI-DIDate4 Aug 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Instrument Table
Model / reference
HULK
Primary DI / UDI-DI
06974998880361
Basic UDI-DI
697499888TableKH
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

Similar devices in this category

Other devices filed under OPHTHALMIC DEVICES - OTHER.

Other devices from Main MediTech Co., Ltd

See all devices from Main MediTech Co., Ltd →

Properties

Other properties (14, all answered No)