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Prelude SNAP™

by Merit Medical Systems, Inc. 45 variants

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 6 Oct 2026. What this means

Overview

The Prelude SNAP device is a non-implantable, invasive device used for vascular catheter introduction into the vascular system. It features a non-steerable introducer sheath with an inner obturator/dilator and additional access devices such as guidewires, introducer needles, syringes, or haemostatic valves to control blood loss.

Regulatory status

as of registry sync 6 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10884450489656 UDI-DI Date15 Nov 2024ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Vascular catheter introduction set, nonimplantable
Model / Ref / Catalog
A, PLSX-1012.5
Primary DI / UDI-DI
10884450489656
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

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No