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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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Handle — 14 UDI-DI variants, MDR (Unintech GmbH)

MD Atlas
Unintech GmbH

Data from EUDAMED, last updated May 31, 2026

Handle

42607060101handlePL

14 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: Unintech GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42607060101handlePL
Device name: Handle
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: Unintech GmbH
SRN: DE-MF-000005136
Country: Germany
Email: info@unintech.de

Variants by status

UDI-DI variants

14 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS7PT802QZ6SMCE8CYH3P59W

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

UNT-I-463004260706010512
UNT-I-3365N04260706010499
UNT-I-140204260706015883
UNT-I-11128604260706010482
UNT-I-679504260706010673
UNT-I-236504260706010468
UNT-I-808004260706010666
UNT-I-80125004260706010680
UNT-I-140304260706015890
UNT-I-828004260706010444
UNT-I-86129004260706010475
UNT-I-140104260706015593
UNT-I-140004260706015586
UNT-I-323104260706010505