Skip to content

Advanced Instrument OsmoPRO MAX

by Advanced Instruments, LLC

Advanced Instrument OsmoPRO MAX is a Class I device made by Advanced Instruments, LLC, listed in FDA GUDID since 18 Jun 2026 (UDI-DI 00816068021150), 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 Number00816068021150 UDI-DI Date18 Jun 2026ListedStatusListed 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  • Withdrawn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

Generic name
Osmometric analyser IVD
Model / Ref / Catalog
OsmoPRO MAX
Primary DI / UDI-DI
00816068021150
FDA product code
JJM
GMDN term
Osmometric analyser IVD
Device class
Class I
Regulation number
862.2730
GUDID distribution status
In Commercial Distribution

From the manufacturer

Manufacturer's product page: Advanced Instruments® OsmoPRO® MAX Automated Osmometer

Similar devices

Other devices filed under FDA product code JJM (Osmometer For Clinical Use).

Other devices from Advanced Instruments, LLC

See all devices from Advanced Instruments, LLC →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)