Skip to content

REFPSM5014C

by Suzhou Health Medical Plastic Products Co., Ltd.

Ref REFPSM5014C

REFPSM5014C is a Class I device made by Suzhou Health Medical Plastic Products Co., Ltd., registered in EUDAMED on 26 Oct 2026 (Basic UDI-DI 06971827340232UB), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number06971827340232UB Basic UDI-DI Date26 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
REFPSM5014C
Primary DI / UDI-DI
(01)06971827340416, (01)16971827340410
Basic UDI-DI
06971827340232UB
EMDN code
A070501 Caps or obturators, non-perforable
Device class
Class I
EU registration type
Standard device
EU market of registration
Finland
Poland

Manufacturer details

EUDAMED SRN
CN-MF-000041302
Authorised representative
HUMISS TRADING S. L. ES-AR-000040177

Similar devices in this category

Other devices filed under CAPS OR OBTURATORS, NON-PERFORABLE.

Other devices from Suzhou Health Medical Plastic Products Co., Ltd.

Properties

  • Supplied sterile
Other properties (13, all answered No)