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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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EyeSuite Myopia — 6 UDI-DI variants, MDR (Haag-Streit AG)

MD Atlas
Haag-Streit AG

Data from EUDAMED, last updated May 23, 2026

EyeSuite Myopia

764013298MyopiaDJ

6 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Haag-Streit AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 764013298MyopiaDJ
Device name: EyeSuite Myopia
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Jun 29, 2023

Manufacturer & authorised representative

Manufacturer

Name: Haag-Streit AG
SRN: CH-MF-000020981
Country: Switzerland
Email: regulatory@haag-streit.com
Phone: +41 31 978 01 11

Authorised representative

Name: Haag-Streit Deutschland GmbH
SRN: DE-AR-000025462
Country: Germany
Phone: +49 4103 709 02

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01GZB3TMNM6Q54FMS53JRHPQJQ

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

102381507640132987782
102381507640132988093
102381507640132989243
102381507640132988802
102381507640132988796
102381507640132988949