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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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Cutting Instruments — 11 UDI-DI variants, MDR (Aprikos Medical AS)

MD Atlas
Aprikos Medical AS

Data from EUDAMED, last updated May 31, 2026

Cutting Instruments

7073371FILE104LD

11 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: Aprikos Medical AS

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 7073371FILE104LD
Device name: Cutting Instruments
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Aprikos Medical AS
SRN: NO-MF-000044411
Country: Norway
Email: info@aprikosmedical.com
Phone: 47 22223400

Variants by status

UDI-DI variants

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSJAXJGWCSZ9YQACPH0NC8HD

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

Aprikos Medical07073371092007
Aprikos Medical07073371092038
Aprikos Medical07073371092045
Aprikos Medical07073371092106
Aprikos Medical07073371092144
Aprikos Medical07073371092113
Aprikos Medical07073371092052
Aprikos Medical07073371092076
Aprikos Medical07073371092021
Aprikos Medical07073371092014
Aprikos Medical07073371092120