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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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Cryo treatment — 2 UDI-DI variants, MDR

MD Atlas
Medical Brands Innovations BV

Data from EUDAMED, last updated May 31, 2026

Cryo treatment

872064878940K3

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Medical Brands Innovations BV

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Device characteristics

Active device

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 872064878940K3
Device name: —
Device model: Cryo treatment
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: Medical Brands Innovations BV
SRN: NL-MF-000008534
Country: Netherlands
Email: qara@medicalbrands.com
Phone: +31 20 345 5330

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS7E55TT8EKKT23XPJCMGB6M

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

150ST.ME.DE04008491125833
150CW.ME.DE04008491109444