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Shrill® JSHPP8000

by Joimax GmbH

Ref JSHPP8000

Shrill® JSHPP8000 is a device classified as Class IIa in the EU and Class I in the US made by Joimax GmbH, registered in EUDAMED on 21 May 2026 (Basic UDI-DI 42503371SHRI2HPJG) and listed in FDA GUDID since 30 Dec 2022 (UDI-DI 04250337112549), active as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number42503371SHRI2HPJG Basic UDI-DI 04250337112549UDI-DIDate21 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04250337112549 UDI-DI Date30 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 42503371SHRI2HPJG registered 21 May 2026 Active
  • FDA GUDID UDI-DI 04250337112549 listed 30 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04250337112549
  2. Registered EUDAMED 42503371SHRI2HPJG

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  • Withdrawn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
joimax® Shaver Hand Piece, plus EUDAMED
Shrill® GUDID
Generic name
Arthroscopic shaver system, electrically-powered
Device name
joimax® Shrill® Shaver Handpiece, large
Model / Ref / Catalog
JSHPP8000
Primary DI / UDI-DI
04250337112549
Basic UDI-DI
42503371SHRI2HPJG
Direct marketing DI
04250337112549
FDA product code
HWE
EMDN code
Z12020201 Motorised systems for endoscopic surgery
GMDN term
Arthroscopic shaver system, electrically-powered
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
878.4820
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
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: Arthroscopic shaver system, electrically-powered

Similar devices in this category

Other devices filed under ENDOSCOPIC AND MINIMALLY INVASIVE SURGERY INSTRUMENTS.

Other devices from Joimax GmbH

See all devices from Joimax GmbH →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (20, all answered No)