Skip to content

Globe Scientific 3826

by Globe Scientific, LLC

Globe Scientific 3826 is a fluid transfer tube (FDA Class I; FDA product code LXG) made by Globe Scientific, LLC, listed in FDA GUDID since 26 Nov 2019 (UDI-DI 00840095606165), 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 Number00840095606165 UDI-DI Date26 Nov 2019ListedStatusListed 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  • Withdrawn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 Scientific
Generic name
Fluid transfer tube, general-purpose
Model / reference
3826
Primary DI / UDI-DI
00840095606165
FDA product code
LXG
GMDN term
Fluid transfer tube, general-purpose
Device class
Class I
Regulation number
862.2050
GUDID distribution status
In Commercial Distribution

Related devices

Category: Fluid transfer tube, general-purpose

Similar devices

Other devices filed under FDA product code LXG (Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use).

Other devices from Globe Scientific, LLC

See all devices from Globe Scientific, LLC →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)