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Globe Scientific 172513

by Globe Scientific, LLC

Globe Scientific 172513 is a Class I device made by Globe Scientific, LLC, listed in FDA GUDID since 26 Nov 2019 (UDI-DI 00840095604420), 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 Number00840095604420 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  • Withdrawn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
Capillary blood collection tube IVD, no additive
Model / reference
172513
Primary DI / UDI-DI
00840095604420
FDA product code
GIO
GMDN term
Capillary blood collection tube IVD, no additive
Device class
Class I
Regulation number
864.6150
GUDID distribution status
In Commercial Distribution

Related devices

Category: Capillary blood collection tube IVD, no additive

Similar devices

Other devices filed under FDA product code GIO (Tube, Collection, Capillary Blood).

Other devices from Globe Scientific, LLC

See all devices from Globe Scientific, LLC →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)