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Advocate™ 00884450302132

by Merit Medical Systems, Inc.

Advocate™ 00884450302132 (A35090040130/A) is a Class II device made by Merit Medical Systems, Inc., listed in FDA GUDID since 1 Dec 2020 (UDI-DI 00884450302132), 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 Number00884450302132 UDI-DI Date1 Dec 2020ListedStatusListed 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  • Withdrawn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
Advocate™
Generic name
Peripheral angioplasty balloon catheter, basic
Model / Ref / Catalog
00884450302132, A35090040130/A
Primary DI / UDI-DI
00884450302132
FDA product code
LIT
GMDN term
Peripheral angioplasty balloon catheter, basic
Device class
Class II
Regulation number
870.1250
GUDID distribution status
In Commercial Distribution

Related devices

Category: Peripheral angioplasty balloon catheter, basic

Other devices from Merit Medical Systems, Inc.

See all devices from Merit Medical Systems, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)