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Quala WEADCELV

by National Distribution & Contracting, Inc.

Quala WEADCELV is a Class I device made by National Distribution & Contracting, Inc., listed in FDA GUDID since 27 Sep 2022 (UDI-DI D023WEADCELV3), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD023WEADCELV3 UDI-DI Date27 Sep 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Quala
Generic name
Patient examination/treatment drape, single-use
Model / Ref / Catalog
WEADCELV
Primary DI / UDI-DI
D023WEADCELV3
FDA product code
KHR
GMDN term
Patient examination/treatment drape, single-use
Device class
Class I
Regulation number
872.6050
GUDID distribution status
In Commercial Distribution

Related devices

Category: Patient examination/treatment drape, single-use

Similar devices

Other devices filed under FDA product code KHR (Absorber, Saliva, Paper).

Other devices from National Distribution & Contracting, Inc.

See all devices from National Distribution & Contracting, Inc. →

Properties

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