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DIAMENTOR chamber, size B

by PTW-Freiburg Physikalisch-Technische Werkstätten Dr. Pychlau GmbH 6 variants

DIAMENTOR chamber, size B (TA34028-1) is a multi-modality therapeutic radiation phantom (FDA Class I; FDA product code LHO, Instrument, Quality-Assurance, Radiologic) made by PTW-Freiburg Physikalisch-Technische Werkstätten Dr. Pychlau GmbH, listed in FDA GUDID since 26 Apr 2017 (UDI-DI EPTWTA34028Y10), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberEPTWTA34028Y10 UDI-DI Date26 Apr 2017ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Diamentor
Generic name
Multi-modality therapeutic radiation phantom, anthropomorphic
Model / Ref / Catalog
DIAMENTOR chamber, size B, TA34028-1
Primary DI / UDI-DI
EPTWTA34028Y10
FDA product code
LHO
GMDN term
Multi-modality therapeutic radiation phantom, anthropomorphic
Device class
Class I
Regulation number
892.1940
GUDID distribution status
In Commercial Distribution

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Properties

  • Prescription use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)