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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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Examining Hook — 8 UDI-DI variants, MDR (Joimax GmbH)

MD Atlas
Joimax GmbH

Data from EUDAMED, last updated May 23, 2026

Examining Hook

42503371PALPHOOHD

8 UDI-DI variants

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

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

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 42503371PALPHOOHD
Device name: Examining Hook
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 29, 2024

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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Export results

Applied filters

basicUdiUlid01HWN38KND9JKTC01HM11FGW3C

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

Examining Hook04250337108825
NiTi Nerve Hook, superelastic04250337116288
NiTi Nerve Hook, superelastic04250337102502
NiTi Nerve Hook, superelastic04250337119623
NiTi Nerve Hook, superelastic04250337117858
NiTi Nerve Hook, superelastic04250337115748
NiTi Nerve Hook, superelastic04250337108344
NiTi Palpation Nerve Hook, superelastic04250337120506