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NA MAM detector

by PTW-Freiburg Physikalisch-Technische Werkstätten Dr. Pychlau GmbH

Ref TL60005

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-+EPTWTL600050 Basic UDI-DI +EPTWTL600050UDI-DIDate15 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number+EPTWTL600050 UDI-DI Date26 Apr 2017ListedStatusListed GUDID: in commercial distribution

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

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Generic Name
Multi-modality therapeutic radiation phantom, anthropomorphic
Device Name
NOMEX MAM detector
Model / Ref / Catalog
TL60005, MAM detector
Primary DI / UDI-DI
+EPTWTL600050 EUDAMED
EPTWTL600050 GUDID
Basic UDI-DI
B-+EPTWTL600050
FDA Product Code
LHO
EMDN Code
Z119002 Dosimeters
GMDN Term
Multi-modality therapeutic radiation phantom, anthropomorphic
Device Class
Class IIb EUDAMED
Class I GUDID
Regulation Number
892.1940
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 3 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
TL60005
GUDID
MAM detector
Primary DI / UDI-DIEUDAMED
+EPTWTL600050
GUDID
EPTWTL600050
Device ClassEUDAMED
Class IIb
GUDID
Class I

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Properties

  • Prescription Use
  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (18)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No