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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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19165 — 4 UDI-DI variants, MDR (Moria S.A.)

MD Atlas
Moria S.A.

Data from EUDAMED, last updated May 19, 2026

19165

37004836lensesL7

4 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: Moria S.A.

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 37004836lensesL7
Device name: 19165
Device model: ALTK applanator lense 7-9-11
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 3, 2025

Manufacturer & authorised representative

Manufacturer

Name: Moria S.A.
SRN: FR-MF-000000336
Country: France
Email: pjay@moria-int.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KBHQ9TCQ8TVZ0WPY6VY6XTZF

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

ALTK applanator lense 6-8-1003700483608164
ALTK applanator lense 7-9-1103700483608157
Applanator lense 7-9 F/LSK C&B03700483608317
Applanator lense 8-10 F/LSK C&B03700483608324