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Autopose Syringe Stand STAND2

by Bimini Technologies LLC

Autopose Syringe Stand STAND2 is a Class I device made by Bimini Technologies LLC, listed in FDA GUDID since 15 Feb 2023 (UDI-DI 00850034511351), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850034511351 UDI-DI Date15 Feb 2023ListedStatusListed 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  • Withdrawn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
Autopose Syringe Stand
Generic name
Surgical container holder
Model / reference
STAND2
Primary DI / UDI-DI
00850034511351
FDA product code
MDM
GMDN term
Surgical container holder
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code MDM (Instrument, Manual, Surgical, General Use).

Other devices from Bimini Technologies LLC

See all devices from Bimini Technologies LLC →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)