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Wet Pack Products

by Shandong Haiyan Medical Manufacture Co., Ltd. 4 variants

Ref P1-IA-3Model P1-IA-1、P1-IA-2、P1-IA-3、P2-IA-1、P2-IA-2

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 Number69565997SSIA8R Basic UDI-DI 06956599700217UDI-DIDate25 Apr 2023RegisteredStatusActive

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  • Withdrawn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
Wet Pack Products
Model / Reference
P1-IA-1、P1-IA-2、P1-IA-3、P2-IA-1、P2-IA-2, P1-IA-3
Primary DI / UDI-DI
06956599700217
Basic UDI-DI
69565997SSIA8R
Direct Marketing DI
06956599700217
EMDN Code
D0702 Isopropyl alcohol for the disinfection of medical devices
Device Class
Class IIa
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000001297
Authorised representative
Lotus NL B.V. NL-AR-000000121

Other devices from Shandong Haiyan Medical Manufacture 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