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AccessPLUS™ T

by Merit Medical Systems, Inc.

Ref MAP152Model G

AccessPLUS™ T (MAP152) is a device classified as Class IIa in the EU and Class II in the US made by Merit Medical Systems, Inc., registered in EUDAMED on 21 Oct 2026 (Basic UDI-DI B-00884450662373) and listed in FDA GUDID since 28 Mar 2025 (UDI-DI 00884450662373), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00884450662373 Basic UDI-DI 00884450662373UDI-DIDate21 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00884450662373 UDI-DI Date28 Mar 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00884450662373 registered 21 Oct 2026 Active
  • FDA GUDID UDI-DI 00884450662373 listed 28 Mar 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00884450662373
  2. Registered EUDAMED B-00884450662373

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
AccessPLUS™
Generic name
Angiography kit
Model / Ref / Catalog
G, MAP152, T, 00884450662373
Primary DI / UDI-DI
00884450662373, 00884450860090
Basic UDI-DI
B-00884450662373
FDA product code
DTL
EMDN code
C900101 Haemostasis valves
GMDN term
Angiography kit
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
870.4290
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
G
MAP152
GUDID
T
00884450662373
Device classEUDAMED
Class IIa
GUDID
Class II

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Angiography kitHaemostasis valve

Similar devices in this category

Other devices filed under HAEMOSTASIS VALVES.

Other devices from Merit Medical Systems, Inc.

See all devices from Merit Medical Systems, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Contains animal tissues or cells
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (18, all answered No)