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Algomed Computerized Pressure Algometer FPIX

by Medoc Corp.

Ref AS 00300

Algomed Computerized Pressure Algometer FPIX (AS 00300) is a pressure algesimeter (EU MDR Class IIa; FDA Class I; FDA product code HRW, Dynamometer, Nonpowered) made by Medoc Corp., registered in EUDAMED on 3 Aug 2026 (Basic UDI-DI 72901030300002EY) and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 07290103039059), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number72901030300002EY Basic UDI-DI 07290103039059UDI-DIDate3 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07290103039059 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 72901030300002EY registered 3 Aug 2026 Active
  • FDA GUDID UDI-DI 07290103039059 listed 24 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07290103039059
  2. Registered EUDAMED 72901030300002EY

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
AlgoMed FPIX System EUDAMED
Algomed Computerized Pressure Algometer GUDID
Generic name
Pressure algesimeter
Model / Ref / Catalog
AS 00300, FPIX
Primary DI / UDI-DI
07290103039059
Basic UDI-DI
72901030300002EY
Direct marketing DI
07290103039059
FDA product code
HRW
EMDN code
V030207 Sensitivity measurements devices not included in other classes
GMDN term
Pressure algesimeter
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
888.1250
EU registration type
Standard device
EU market of registration
Denmark
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
AS 00300
GUDID
FPIX
Device classEUDAMED
Class IIa
GUDID
Class I

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Pressure algesimeter

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Properties

  • Reusable
  • Measuring function
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (20, all answered No)