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Asp Global PFG200S-Bio

by Asp Global, LLC

Asp Global PFG200S-Bio is a Class I device made by Asp Global, LLC, listed in FDA GUDID since 5 Sep 2023 (UDI-DI 00840216123311), 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 Number00840216123311 UDI-DI Date5 Sep 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  • Withdrawn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

Trade name
Asp Global
Generic name
Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Model / reference
PFG200S-BIO
Primary DI / UDI-DI
00840216123311
FDA product code
LZA, LZC, QDO, OPJ
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 Asp Global, LLC

See all devices from Asp Global, LLC →

Properties

  • Single use
  • Contains latex
  • Premarket exempt
Other properties (12, all answered No)