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OSMETTE Printer Ribbon 2053

by Precision Systems, Inc.

OSMETTE Printer Ribbon 2053 is a Class I device made by Precision Systems, Inc., listed in FDA GUDID since 14 Oct 2023 (UDI-DI 00850041049564), 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 Number00850041049564 UDI-DI Date14 Oct 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  • Withdrawn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
OSMETTE Printer Ribbon
Generic name
Osmolality IVD, kit, freezing point
Model / Ref / Catalog
2053
Primary DI / UDI-DI
00850041049564
FDA product code
JJM
GMDN term
Osmolality IVD, kit, freezing point
Device class
Class I
Regulation number
862.2730
GUDID distribution status
In Commercial Distribution

Related devices

Category: Osmolality IVD, kit, freezing point

Similar devices

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

Other devices from Precision Systems, Inc.

See all devices from Precision Systems, Inc. →

Properties

  • Premarket exempt
Other properties (14, all answered No)