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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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Rescue Blanket — 2 UDI-DI variants, MDR (1M4 OÜ)

MD Atlas
1M4 OÜ

Data from EUDAMED, last updated May 23, 2026

Rescue Blanket

474501056410022BA

2 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: 1M4 OÜ

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 474501056410022BA
Device name: Rescue Blanket
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 6, 2025

Manufacturer & authorised representative

Manufacturer

Name: 1M4 OÜ
SRN: EE-MF-000040367
Country: Estonia
Email: info@1m4.eu

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JNN0F50HG5F7Q5DK1GVAY6CX

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

10022.0104745010564246
10022.0204745010564253