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dr.green's

by Aden Medi̇kal Ci̇hazlar Ve Aletler İth.i̇hra. Paz.san.ti̇c.ltd.sti. 85 variants

Ref DG-6000

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8699158401207FP Basic UDI-DI 08699158401207UDI-DIDate25 May 2026RegisteredStatusActive

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  • Withdrawn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
(Impervious Set) Percutaneous Drape Pack
Model / Reference
DG-6000
Primary DI / UDI-DI
08699158401207
Basic UDI-DI
8699158401207FP
EMDN Code
T020102 Specialistic surgery drapes
Device Class
Class I
Medical Purpose
Used in Urological Operations such as Nephrology surgery and examinations.

Manufacturer details

EUDAMED SRN
TR-PR-000050110

Other devices from Aden Medi̇kal Ci̇hazlar Ve Aletler İth.i̇hra. Paz.san.ti̇c.ltd.sti.

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Properties

  • Sterile