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LLD 129 Basic

by Drtech Corp.

LLD 129 Basic is a Class I device made by Drtech Corp., listed in FDA GUDID since 3 Nov 2023 (UDI-DI 08800018421307), registry data as of 21 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 21 Oct 2026.

Regulatory status

as of registry sync 21 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08800018421307 UDI-DI Date3 Nov 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  • Withdrawn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

Generic name
X-ray film cassette holder
Model / reference
LLD 129 Basic
Primary DI / UDI-DI
08800018421307
FDA product code
IXY
GMDN term
X-ray film cassette holder
Device class
Class I
Regulation number
892.1880
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 Drtech Corp.

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Properties

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