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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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OST — 6 UDI-DI variants, MDR (ESSILOR INTERNATIONAL)

MD Atlas
ESSILOR INTERNATIONAL

Data from EUDAMED, last updated May 19, 2026

OST

361502000000IOST0000000DX

6 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: ESSILOR INTERNATIONAL

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 361502000000IOST0000000DX
Device name: OST
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: ESSILOR INTERNATIONAL
SRN: FR-MF-000007175
Country: France
Email: info@essilor.fr
Phone: + 33 1 49 77 42 24

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01K2MHA042G3T4HV2N242VM3CH

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

OST10003615020000472
OST 15003615020000489
OST 25003615020000502
OST 250 C03615020000755
OST 250 H03615020000762
OST 35003615020000779