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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 27 Dec 2016 (UDI-DI 00748426066544), 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 Number00748426066544 UDI-DI Date27 Dec 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  • Withdrawn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
Instrument/equipment drape, single-use, sterile
Model / reference
1
Primary DI / UDI-DI
00748426066544
FDA product code
KKX
GMDN term
Instrument/equipment drape, single-use, sterile
Device class
Class II
Regulation number
878.4370
GUDID distribution status
In Commercial Distribution

Related devices

Category: Instrument/equipment drape, single-use, sterile

Similar devices in this category

Other devices filed under Instrument/equipment drape, single-use, sterile.

Other devices from Microtek Medical LLC

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Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)