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Globe® Loader Plug 601-01006

by Kardium Inc

Globe® Loader Plug 601-01006 (PLU01GL01) is a Class II device made by Kardium Inc, listed in FDA GUDID since 17 Sep 2026 (UDI-DI 07540162100574), 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 Number07540162100574 UDI-DI Date17 Sep 2026ListedStatusListed 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  • Withdrawn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
Globe® Loader Plug
Generic name
Stopcock
Model / Ref / Catalog
601-01006, PLU01GL01
Primary DI / UDI-DI
07540162100574
FDA product code
DTL
GMDN term
Stopcock
Device class
Class II
Regulation number
870.4290
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code DTL (Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass).

Other devices from Kardium Inc

See all devices from Kardium Inc →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)