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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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Ear Curetters, Knives — 82 UDI-DI variants, MDR (Aprikos Medical AS)

MD Atlas
Aprikos Medical AS

Data from EUDAMED, last updated May 31, 2026

Ear Curetters, Knives

7073371FILE106LH

82 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: 7073371FILE106LH
Device name: Ear Curetters, Knives
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

82 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSJAXM35VV875WQ8BERN5AZF

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 Medical07073371095442
Aprikos Medical07073371096180
Aprikos Medical07073371094988
Aprikos Medical07073371096142
Aprikos Medical07073371096203
Aprikos Medical07073371096067
Aprikos Medical07073371095893

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