Skip to content

Cak

by Changzhou Ankang Medical Instruments Co., Ltd. 9 variants

Ref AKYGCA-32/33/34/36, AKYGCB-32/33/34/36

Active European Union

CE MDD

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-69532408004T98A Basic UDI-DI D-69532408004T98AUDI-DIDate31 Jul 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Disposable Prolapse Hemorrhoids Staplers
Model / Reference
AKYGCA-32/33/34/36, AKYGCB-32/33/34/36
Primary DI / UDI-DI
D-69532408004T98A
Basic UDI-DI
B-69532408004T98A
EMDN Code
H0202020101 Single-use straight circular staplers for open surgery
Device Class
Class IIb
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
CN-MF-000001163
Authorised representative
Lotus NL B.V. NL-AR-000000121

Other devices from Changzhou Ankang Medical Instruments Co., Ltd.

See all devices from Changzhou Ankang Medical Instruments Co., Ltd. →

Properties

  • Sterile
  • Implantable

Other properties (9)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No