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dose-map™ Biobeam 2000 Custom

by Ashland Specialty Ingredients, G.P.

dose-map™ Biobeam 2000 Custom (943965) is a Class II device made by Ashland Specialty Ingredients, G.P., listed in FDA GUDID since 10 May 2023 (UDI-DI 00810106410579), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810106410579 UDI-DI Date10 May 2023ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
dose-map™
Generic name
X-ray film cassette holder
Model / Ref / Catalog
Biobeam 2000 Custom, 943965
Primary DI / UDI-DI
00810106410579
FDA product code
IXA
GMDN term
X-ray film cassette holder
Device class
Class II
Regulation number
892.1850
GUDID distribution status
In Commercial Distribution

Related devices

Category: X-ray film cassette holder

Similar devices in this category

Other devices filed under X-ray film cassette holder.

Other devices from Ashland Specialty Ingredients, G.P.

See all devices from Ashland Specialty Ingredients, G.P. →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)