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Sponge Pad

by Tianjin Zhengtian Medical Instrument Co., Ltd.

Ref CS010435, CS100401

Sponge Pad (CS010435) is a Class I device made by Tianjin Zhengtian Medical Instrument Co., Ltd., registered in EUDAMED on 19 Sep 2024 (Basic UDI-DI B-CNMF0000201150630HL), active as of 22 Oct 2026.

Active European Union

CE MDD

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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-CNMF0000201150630HL Basic UDI-DI Date19 Sep 2024RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Sponge Pad
Model / reference
CS010435, CS100401
Primary DI / UDI-DI
D-CNMF0000201150630HL, D-CNMF0000201150638J4
Basic UDI-DI
B-CNMF0000201150630HL, B-CNMF0000201150638J4
EMDN code
L091199 Orthopaedic prosthetics instruments, reusable - other
Device class
Class I
EU registration type
Legacy device (under a directive)
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
CN-MF-000020115
Authorised representative
Inion Oy FI-AR-000046224

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER.

Other devices from Tianjin Zhengtian Medical Instrument Co., Ltd.

See all devices from Tianjin Zhengtian Medical Instrument Co., Ltd. →

Properties

  • Sterilise before use
  • Reusable
Other properties (10, all answered No)