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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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Dino-Lite DermaScope — 5 UDI-DI variants, MDR (IDCP BV)

MD Atlas
IDCP BV

Data from EUDAMED, last updated May 30, 2026

Dino-Lite DermaScope

87202991629MEDLD8K

5 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: IDCP BV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 87202991629MEDLD8K
Device name: Dino-Lite DermaScope
Device model: Dino-Lite DermaScope
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 15, 2025

Manufacturer & authorised representative

Manufacturer

Name: IDCP BV
SRN: NL-MF-000000755
Country: Netherlands
Email: jan.boers@idcp.nl
Phone: +31206186322

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01JV4HYS68TJXKZACSCN38DVB7

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

Dino-Lite DermaScope08721325045034
Dino-Lite DermaScope08721325045003
Dino-Lite DermaScope08721325045010
Dino-Lite DermaScope08721325045027
Dino-Lite DermaScope08721325045041