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Merlin™ 3638

by St. Jude Medical, Inc.

Merlin™ 3638 is a Class III device made by St. Jude Medical, Inc., listed in FDA GUDID since 3 Feb 2017 (UDI-DI 05414734502078), 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 Number05414734502078 UDI-DI Date3 Feb 2017ListedStatusListed 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  • Withdrawn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
Merlin™
Generic name
Multiple active implantable device programmer
Model / Ref / Catalog
3638
Primary DI / UDI-DI
05414734502078
FDA product code
NVZ
GMDN term
Multiple active implantable device programmer
Device class
Class III
GUDID distribution status
In Commercial Distribution

Related devices

Category: Multiple active implantable device programmer

Similar devices

Also classified as Multiple active implantable device programmer.

Other devices from St. Jude Medical, Inc.

See all devices from St. Jude Medical, Inc. →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)