← Back to catalogue

joimax® Shrill® Shaver Handpiece large

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref JSHRI02SHL

by Joimax GmbH

Identity

Trade Name
joimax® Shrill® Shaver Handpiece large EUDAMED
joimax® Shrill® Shaver Handpiece, large EUDAMED
Shrill® FDA UDI
Generic Name
Arthroscopic shaver system, electrically-powered FDA UDI
Device Name
joimax® Shrill® Shaver Handpiece large EUDAMEDFDA UDI
joimax® Shrill® Shaver Handpiece, large EUDAMED
Model / Reference
JSHRI02SHL EUDAMEDFDA UDI
Description
joimax® Shrill® Shaver Handpiece large FDA UDI

Identifiers

Catalog Number
JSHRI02SHL FDA UDI
Primary DI / UDI-DI
04250337118800 EUDAMEDFDA UDI
Basic UDI-DI
B-04250337118800 EUDAMED
42503371SHRI2HPJG EUDAMED
Direct Marketing DI
04250337118800 EUDAMED
FDA Product Code
HWE FDA UDI
EMDN Code
Z12020201 MOTORISED SYSTEMS FOR ENDOSCOPIC SURGERY EUDAMED
GMDN Term
Arthroscopic shaver system, electrically-powered FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
878.4820 FDA UDI
Market of Registration
Spain EUDAMED
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

joimax® Shrill® Shaver Handpiece large by Joimax GmbH — Class IIa — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Joimax GmbH
EUDAMED SRN
DE-MF-000009201

Sources (3)

  • EUDAMED 4664605b-1097-4352-a748-9b4242da158f 61 fields · synced Sep 17, 2026
  • FDA UDI cb1d716a-8e6c-4c7f-b20a-0ebc123c6c10 35 fields · synced May 30, 2026
  • EUDAMED 4e8bf228-acdd-4de7-aa7b-9306c0be27e3 61 fields · synced Sep 17, 2026