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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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VIDEOCOLPOSCOPE — 2 UDI-DI variants, MDR (OPTOMIC ESPAÑA S.A)

MD Atlas
OPTOMIC ESPAÑA S.A

Data from EUDAMED, last updated May 23, 2026

VIDEOCOLPOSCOPE

84360415801152K

2 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: OPTOMIC ESPAÑA S.A

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 84360415801152K
Device name: VIDEOCOLPOSCOPE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 14, 2026

Manufacturer & authorised representative

Manufacturer

Name: OPTOMIC ESPAÑA S.A
SRN: ES-MF-000003235
Country: Spain
Email: prrc@optomic.com
Phone: +34 91 804 44 44

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRJZAMQJF6KZFH0TTN31SS4H

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

1965700108436041581499
1966700108436041581598