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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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Masalo Manschette MED — 4 UDI-DI variants, MDR (MASALO KG)

MD Atlas
MASALO KG

Data from EUDAMED, last updated May 23, 2026

Masalo Manschette MED

42516685MMMEDMM

4 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: MASALO KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42516685MMMEDMM
Device name: Masalo Manschette MED
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 10, 2026

Manufacturer & authorised representative

Manufacturer

Name: MASALO KG
SRN: DE-MF-000014041
Country: Germany
Email: shop@masalo.eu
Phone: +49 4131 727 15 97

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KKC1GEYQEPX3DZJNK6CXC2ZR

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

MMMEDG-1L04251668500012
MMMEDG-2R04251668500043
MMMEDG-1R04251668500029
MMMEDG-2L04251668500036