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Globe Scientific 5913

by Globe Scientific, LLC

Globe Scientific 5913 is a Class I device made by Globe Scientific, LLC, listed in FDA GUDID since 26 Nov 2019 (UDI-DI 00840095608053), 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 Number00840095608053 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  • Withdrawn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
General specimen container IVD, no additive, sterile
Model / reference
5913
Primary DI / UDI-DI
00840095608053
FDA product code
FMH
GMDN term
General specimen container IVD, no additive, sterile
Device class
Class I
Regulation number
864.3250
GUDID distribution status
In Commercial Distribution

Related devices

Category: General specimen container IVD, no additive, sterile

Other devices from Globe Scientific, LLC

See all devices from Globe Scientific, LLC →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)