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Sjm™ 406304

by St. Jude Medical, Inc.

Sjm™ 406304 is a Class II device made by St. Jude Medical, Inc., listed in FDA GUDID since 30 Apr 2015 (UDI-DI 05414734027038), 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 Number05414734027038 UDI-DI Date30 Apr 2015ListedStatusListed 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  • Withdrawn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
Sjm™
Generic name
Haemostasis valve
Model / Ref / Catalog
406304
Primary DI / UDI-DI
05414734027038
FDA product code
DYB
GMDN term
Haemostasis valve
Device class
Class II
Regulation number
870.1340
GUDID distribution status
In Commercial Distribution
Size
Catheter Gauge — 9 French

Related devices

Category: Haemostasis valve

Similar devices in this category

Other devices filed under Haemostasis valve.

Other devices from St. Jude Medical, Inc.

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

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)