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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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Organization name
UDI-DI code
Reference / catalog number

NT-820MVU — Class I MDR by NODIN Aviation AS

MD Atlas
NODIN Aviation AS

EUDAMED last updated this device on Apr 30, 2026

NT-820MVU

709006732NT-820MVUM8

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: NODIN Aviation AS
UDI-DI code: 07090067320008
Reference / catalog number: NT-820MVU

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View device family (Basic UDI)

Manufacturer information

Organization name: NODIN Aviation AS
SRN: NO-MF-000053277
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Norway; available across 1 country total.

Country	On market since	Until
NorwayPrimary placement	Nov 27, 2024	Still on market

Device identification

Trade name: not provided
UDI-DI code: 07090067320008
Basic UDI-DI: 709006732NT-820MVUM8
Reference / catalog number: NT-820MVU
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: The NODIN 4-Folded MEDEVAC Stretcher is developed according to NATO Standard 2040, (Stretchers, Bearing Brackets and Attachment Supports) as well as STANAG 3204 AMD, (Aero medical Evacuation), Annex E, to facilitate safe transport of patients by land vehicles, naval vessels or aerial vehicles.
Additional information URL: https://medevac.no/product/nt-820mvu/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)07090067320008

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

V08050101GENERIC USE STRETCHERS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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Related devices

This device is not currently linked to any other device.

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.