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Innomed

by Zhejiang Longterm Medical Technology Co., Ltd. 192 variants

Ref G4101

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number692636552000682 Basic UDI-DI 06926365587915UDI-DIDate9 Jan 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Hydrogel dressing
Model / Reference
G4101
Primary DI / UDI-DI
06926365587915
Basic UDI-DI
692636552000682
Direct Marketing DI
06926365587915
EMDN Code
M04040501 Hydrogel dressings, non-combined
Device Class
Class IIb
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
CN-MF-000001161
Authorised representative
Lotus NL B.V. NL-AR-000000121

Other devices from Zhejiang Longterm Medical Technology Co., Ltd.

See all devices from Zhejiang Longterm Medical Technology Co., Ltd. →

Properties

  • Sterile

Other properties (12)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No