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LLD 129 Compact

by Drtech Corp.

LLD 129 Compact is a Class I device made by Drtech Corp., listed in FDA GUDID since 12 Apr 2023 (UDI-DI 08800018421000), registry data as of 31 May 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 31 May 2026.

Regulatory status

as of registry sync 31 May 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08800018421000 UDI-DI Date12 Apr 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  • Withdrawn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 Compact
Primary DI / UDI-DI
08800018421000
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.

See all devices from Drtech Corp. →

Properties

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