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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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HYPO — 8 UDI-DI variants, MDR (LAUDA Medical GmbH & Co. KG)

MD Atlas
LAUDA Medical GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

HYPO

426248181HYPODY

8 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: LAUDA Medical GmbH & Co. KG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426248181HYPODY
Device name: HYPO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: LAUDA Medical GmbH & Co. KG
SRN: DE-MF-000027737
Country: Germany
Email: support@lauda-medical.com

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRE2FPB2GJPN4R0H9RQAAXNM

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

LM00009704262481810158
LM00009504262481810202
LM00009404262481810196
LM00009304262481810189
LM00009204262481810172
LM00009104262481810165
LM00009604262481810219
LM00009004262481810141