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TrollByte Kimera Red 2405

by Directa AB

TrollByte Kimera Red 2405 (1572240503) is a Class I device made by Directa AB, listed in FDA GUDID since 6 Dec 2022 (UDI-DI 17310230005813), 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 Number17310230005813 UDI-DI Date6 Dec 2022ListedStatusListed 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  • Withdrawn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
TrollByte
Generic name
Dental x-ray film holder, reusable
Model / Ref / Catalog
Kimera Red 2405, 1572240503
Primary DI / UDI-DI
17310230005813
FDA product code
EGZ
GMDN term
Dental x-ray film holder, reusable
Device class
Class I
Regulation number
872.1905
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code EGZ (Holder, Film, X-Ray).

Other devices from Directa AB

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Properties

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