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SmartPractice AL925

by Smarthealth, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 8 Nov 2026. What this means

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00854498007542 UDI-DI Date16 Dec 2020ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
SmartPractice
Generic name
General laboratory container, reusable
Model / Ref / Catalog
AL925
Primary DI / UDI-DI
00854498007542
FDA product code
LXG
GMDN term
General laboratory container, reusable
Device class
Class I
Regulation number
862.2050
GUDID distribution status
In Commercial Distribution

Related devices

Category: General laboratory container, reusable

Other devices from Smarthealth, Inc.

See all devices from Smarthealth, Inc. →

Properties

  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date

Other properties (11)

  • Supplied sterile: No
  • Sterilise before use: No
  • Single use: No
  • Implantable: No
  • Contains latex: No
  • Prescription use: No
  • Over-the-counter: No
  • Combination product: No
  • HCT/P: No
  • Serial number: No
  • Manufacturing date: No