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microfet handgrip 5050-100

by Hoggan Scientific L.L.C.

Part of a family of 16 devices: see the family page

Ref 5050-100

microfet handgrip 5050-100 is a hand dynamometer/pinchmeter (EU MDR Class I; FDA Class II; FDA product code LBB, Dynamometer, Ac-Powered) made by Hoggan Scientific L.L.C., registered in EUDAMED on 31 Aug 2026 (Basic UDI-DI 850002429microFETHP) and listed in FDA GUDID since 25 Feb 2025 (UDI-DI 00850002429114), 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 Number850002429microFETHP Basic UDI-DI 00850002429114UDI-DIDate31 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00850002429114 UDI-DI Date25 Feb 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 850002429microFETHP registered 31 Aug 2026 Active
  • FDA GUDID UDI-DI 00850002429114 listed 25 Feb 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00850002429114
  2. Registered EUDAMED 850002429microFETHP

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  • Withdrawn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
microfet handgrip
Generic name
Hand dynamometer/pinchmeter, electronic
Model / reference
5050-100
Primary DI / UDI-DI
00850002429114
Basic UDI-DI
850002429microFETHP
FDA product code
LBB
EMDN code
Z12062680, Z12062692
GMDN term
Hand dynamometer/pinchmeter, electronic
Device class
Class I EUDAMED
Class II GUDID
Regulation number
888.1240
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

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

Related devices

Category: Hand dynamometer/pinchmeter, electronic

Similar devices in this category

Other devices filed under DYNAMOMETRIC SYSTEMS FOR MOVEMENT ANALYSIS.

Other devices from Hoggan Scientific, LLC

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Properties

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