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Microtek 1

by Microtek Medical LLC 1,000+ variants

Microtek 1 is a Class II device made by Microtek Medical LLC, listed in FDA GUDID since 4 Nov 2016 (UDI-DI 00748426014552), 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 Number00748426014552 UDI-DI Date4 Nov 2016ListedStatusListed 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  • Withdrawn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
Microtek
Generic name
X-ray system cover
Model / reference
1
Primary DI / UDI-DI
00748426014552
FDA product code
KKX
GMDN term
X-ray system cover
Device class
Class II
Regulation number
878.4370
GUDID distribution status
In Commercial Distribution
Sterilisation method
Radiation Sterilization

Related devices

Category: X-ray system cover

Similar devices

Also classified as X-ray system cover.

Similar devices

Other devices filed under FDA product code KKX (Drape, surgical).

Other devices from Microtek Medical LLC

See all devices from Microtek Medical LLC →

Properties

  • Supplied sterile
  • Sterilise before use
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)