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AccessPLUS™ 00884450590263

by Merit Medical Systems, Inc.

AccessPLUS™ 00884450590263 (MAP150/D) is a Class II device made by Merit Medical Systems, Inc., listed in FDA GUDID since 5 Mar 2022 (UDI-DI 00884450590263), 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 Number00884450590263 UDI-DI Date5 Mar 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  • Withdrawn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
AccessPLUS™
Generic name
Angiography kit
Model / Ref / Catalog
00884450590263, MAP150/D
Primary DI / UDI-DI
00884450590263
FDA product code
DTL
GMDN term
Angiography kit
Device class
Class II
Regulation number
870.4290
GUDID distribution status
In Commercial Distribution

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Category: Angiography kitHaemostasis valve

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Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)