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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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Accessory intended use — 12 UDI-DI variants, MDR (Jaeger Medical GmbH)

MD Atlas
Jaeger Medical GmbH

Data from EUDAMED, last updated May 23, 2026

Accessory intended use

42508929011871QH

12 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: Jaeger Medical GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42508929011871QH
Device name: Accessory intended use
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 7, 2022

Manufacturer & authorised representative

Manufacturer

Name: Jaeger Medical GmbH
SRN: DE-MF-000007090
Country: Germany
Email: jared.cardon@jaegerrdx.com
Phone: +49 931 4972 111

Variants by status

UDI-DI variants

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FJVSJZZ7AXABXY942RHYA5DW

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

V-70739214250892907540
V-70739214250892903726
V-85255614250892903276
V-70772214250892907311
V-70805214250892903580
V-70805214250892907847
V-85255614250892907304
V-70772214250892903269
V-70717514250892905430
V-70805214250892909100
V-70717514250892908899
V-70732714250892903603