Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

joimax® Arthroscope Combo — 10 UDI-DI variants, MDR (Joimax GmbH)

MD Atlas
Joimax GmbH

Data from EUDAMED, last updated May 23, 2026

joimax® Arthroscope Combo

42503371ENSCARTFV

10 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Joimax GmbH

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42503371ENSCARTFV
Device name: joimax® Arthroscope Combo
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: Joimax GmbH
SRN: DE-MF-000009201
Country: Germany
Email: quality@joimax.com
Phone: +49 721 255 14 311

Variants by status

UDI-DI variants

10 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KS4TZ9DTX31B0BAA7A088W5T

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Biportal Laminoscope, ocular04250337120643
Biportal Laminoscope, ocular04250337120605
Biportal Laminoscope, ocular04250337120308
FHD Nucleoscope (2.7 mm OD) Combo04250337105794
FHD Nucleoscope (2.7 mm OD) Ocular04250337105800
FHD Nucleoscope (1,9 mm OD) Ocular04250337109679
FHD Nucleoscope (1.9 mm OD), Combo04250337109662
joimax® Arthroscope Combo04250337100034
joimax® Arthroscope Combo04250337100041
joimax® Arthroscope Combo04250337100027