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PatientCare 5002-0130

by Wallac Oy

PatientCare 5002-0130 is a Class I device made by Wallac Oy, listed in FDA GUDID since 25 Feb 2019 (UDI-DI 06438147153275), registry data as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06438147153275 UDI-DI Date25 Feb 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  • Withdrawn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
PatientCare
Generic name
Clinical laboratory information system
Model / Ref / Catalog
5002-0130
Primary DI / UDI-DI
06438147153275
FDA product code
JQP
GMDN term
Clinical laboratory information system
Device class
Class I
Regulation number
862.2100
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code JQP (Calculator/Data Processing Module, For Clinical Use).

Other devices from Wallac Oy

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Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)