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Protective Sheet

by Ningbo Transo-Medical Co., Ltd. 4 variants

Ref TM3750BModel TM1209, TM1210

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697461841TMPSTS Basic UDI-DI 06974618411470UDI-DIDate15 Oct 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Protection Sheet
Model / Reference
TM1209, TM1210, TM3750B
Primary DI / UDI-DI
06974618411470
Basic UDI-DI
697461841TMPSTS
EMDN Code
T04010299 Absorbent underpads - other
Device Class
Class I
EU market of registration
Sweden

Manufacturer details

EUDAMED SRN
CN-MF-000009687
Authorised representative
Caretechion GmbH DE-AR-000005946

Other devices from Ningbo Transo-Medical Co., Ltd.

See all devices from Ningbo Transo-Medical Co., Ltd. →

Properties

Other properties (13)

  • Sterile: No
  • 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