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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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NODIN 4-Folded MEDEVAC Stretcher — 1 UDI-DI variant, MDR

MD Atlas
NODIN Aviation AS

Data from EUDAMED, last updated May 31, 2026

NODIN 4-Folded MEDEVAC Stretcher

709006732NT-820MVUM8

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: NODIN Aviation AS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 709006732NT-820MVUM8
Device name: NODIN 4-Folded MEDEVAC Stretcher
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 17, 2026

Manufacturer & authorised representative

Manufacturer

Name: NODIN Aviation AS
SRN: NO-MF-000053277
Country: Norway
Email: post@medevac.no
Phone: +47 33327943

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KPD6K20XG2B7C58FMJH2J692

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

NT-820MVU07090067320008