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Advancare ANBM10035

by Intco Medical Industries, Inc.

Advancare ANBM10035 is a Class I device made by Intco Medical Industries, Inc., listed in FDA GUDID since 15 Nov 2023 (UDI-DI B845ANBM100351), 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 NumberB845ANBM100351 UDI-DI Date15 Nov 2023ListedStatusListed 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  • Withdrawn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
Advancare
Generic name
Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Model / Ref / Catalog
ANBM10035
Primary DI / UDI-DI
B845ANBM100351
FDA product code
LZA, LZC
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 Intco Medical Industries, Inc.

See all devices from Intco Medical Industries, Inc. →

Properties

  • Single use
  • Over-the-counter
Other properties (13, all answered No)