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Prelude EASE™ 10884450257927

by Merit Medical Systems, Inc.

Prelude EASE™ 10884450257927 is a Class II device made by Merit Medical Systems, Inc., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 10884450257927), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10884450257927 UDI-DI Date24 Sep 2016ListedStatusListed 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  • Withdrawn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
Prelude EASE™
Generic name
Vascular catheter introduction set, nonimplantable
Model / reference
10884450257927
Primary DI / UDI-DI
10884450257927
FDA product code
DYB
GMDN term
Vascular catheter introduction set, nonimplantable
Device class
Class II
Regulation number
870.1340
GUDID distribution status
In Commercial Distribution

Related devices

Category: Vascular catheter introduction set, nonimplantable

Similar devices in this category

Other devices filed under Vascular catheter introduction set, nonimplantable.

Other devices from Merit Medical Systems, Inc.

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Properties

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