Skip to content

PE Apron

by Ningbo Greetmed Medical Instruments Co., Ltd. 4 variants

Ref GT060-101

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69586275GT060-101VH Basic UDI-DI 06958627537420UDI-DIDate3 Jul 2026RegisteredStatusActive

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  • Withdrawn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
Plastic apron
Model / Reference
GT060-101
Primary DI / UDI-DI
06958627537420
Basic UDI-DI
69586275GT060-101VH
EMDN Code
T0209 Surgical aprons (excluding personal protective equipment - PPE)
Device Class
Class I
Market of Registration
Lithuania

Manufacturer details

EUDAMED SRN
CN-MF-000009634
Authorised representative
MedPath GmbH DE-AR-000000087

Other devices from Ningbo Greetmed Medical Instruments Co., Ltd.

See all devices from Ningbo Greetmed Medical Instruments Co., Ltd. →

Properties

Other properties (13)

  • Sterile: No
  • 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