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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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Manschetten, EM — 34 UDI-DI variants, MDR (HILOTHERM GmbH)

MD Atlas
HILOTHERM GmbH

Data from EUDAMED, last updated May 23, 2026

Manschetten, EM

42503871MANEMFP

34 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: HILOTHERM GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42503871MANEMFP
Device name: Manschetten, EM
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 15, 2025

Manufacturer & authorised representative

Manufacturer

Name: HILOTHERM GmbH
SRN: DE-MF-000006176
Country: Germany
Email: info@hilotherm.com
Phone: +49 (0)7566 91199

Variants by status

UDI-DI variants

34 UDI-DI variants

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Applied filters

basicUdiUlid01KCH71KNG737SMN42ACGRMAKM

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

Round Cuff single-patient use04250387100497
Round cuff, single-patient use-W04250387101739
Small Round Cuff single-patient use04250387100480
Small round cuff, single patient use-W04250387101722
Small Surface Cuff single-patient use04250387100534
Small surface cuff, single patient use-W04250387101753
Trapeze Cuff single-patient use04250387101173
Universal cuff mini single-patient use04250387101135
Upper Face Cuff single-patient use04250387100558

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