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

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Trial Implant Cages 08 — 8 UDI-DI variants, MDR (Joimax GmbH)

MD Atlas
Joimax GmbH

Data from EUDAMED, last updated May 23, 2026

Trial Implant Cages 08

42503371INCATRIEC

8 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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42503371INCATRIEC
Device name: Trial Implant Cages 08
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

8 UDI-DI variants

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Applied filters

basicUdiUlid01KS4V8JFSGX8NS1NEMQKKBSY2

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

Trial Implant Cages 0804250337111139
Trial Implant Cages 0904250337111146
Trial Implant Cages 1004250337111153
Trial Implant Cages 1104250337111160
Trial Implant Cages 1204250337111177
Trial Implant Cages 1304250337111184
Trial Implant Cages 1404250337111191
Trial Inserter04250337112990