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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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Oculoo Eye Drop Glasses — 2 UDI-DI variants, MDR (Oculoo B.V.)

MD Atlas
Oculoo B.V.

Data from EUDAMED, last updated May 31, 2026

Oculoo Eye Drop Glasses

8721593106EDG001ZJ

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: Oculoo B.V.

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 8721593106EDG001ZJ
Device name: Oculoo Eye Drop Glasses
Device model: EDG001
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Oculoo B.V.
SRN: NL-MF-000054845
Country: Netherlands
Email: contact@oculoo.nl
Phone: +31 6 19 04 16 27

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KSMV032RH37GFVARJC8W2HP9

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

Oculoo Eye Drop Glasses08721593106000
Oculoo Minim Eye Drop Glasses08721593106017