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Select Choice NTX0200

by Hemasource

Select Choice NTX0200 is a Class I device made by Hemasource, listed in FDA GUDID since 8 Dec 2022 (UDI-DI 00810045480008), 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 Number00810045480008 UDI-DI Date8 Dec 2022ListedStatusListed 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  • Withdrawn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
Select Choice
Generic name
Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Model / reference
NTX0200
Primary DI / UDI-DI
00810045480008
FDA product code
LZA
GMDN term
Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Device class
Class I
Regulation number
880.6250
GUDID distribution status
In Commercial Distribution

Related devices

Category: Nitrile examination/treatment glove, non-powdered, non-antimicrobial

Similar devices

Other devices filed under FDA product code LZA (Polymer Patient Examination Glove).

Other devices from Hemasource

See all devices from Hemasource →

Properties

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