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Pt-Lt

by PATH MEDICAL GmbH

Part of a family of 27 devices: see the family page

Ref 101014Model 100120

Pt-Lt (101014) is a Class IIa device made by PATH medical GmbH, registered in EUDAMED on 28 May 2026 (Basic UDI-DI 0426022Probes-2aTM), active as of 24 Oct 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0426022Probes-2aTM Basic UDI-DI 04260223144936UDI-DIDate28 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Ep-Te
Model / reference
100120, 101014
Primary DI / UDI-DI
04260223144936
Basic UDI-DI
0426022Probes-2aTM
EMDN code
Z12140380, Z12149001
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000006935

Similar devices in this category

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Properties

Other properties (14, all answered No)