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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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Oculade — 32 UDI-DI variants, MDR

MD Atlas
S.A.L.F. S.p.A. Laboratorio Farmacologico

Data from EUDAMED, last updated May 30, 2026

Oculade

805274210OculadZJ

32 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Manufacturer: S.A.L.F. S.p.A. Laboratorio Farmacologico

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UDI-DI variants

32 UDI-DI variants

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Applied filters

basicUdiUlid01H7CH4D7MHCW73BDHKTN774TM

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

Oculade08052742101677
Oculade08052742101493
Oculade08052742101639
Oculade08052742101653
Oculade08052742101738
Oculade08052742101479
Oculade08052742101554
Oculade08052742101714
Oculade08052742101455
Oculade08052742101691
Oculade08052742101530
Oculade08052742101615
Oculade08052742101516
Oculade08052742101592
Oculade08052742101752
Oculade08052742101578
YaluVISTA®08052742101721
YaluVISTA®08052742101684
YaluVISTA®08052742101509
YaluVISTA®08052742101622
YaluVISTA®08052742101523
YaluVISTA®08052742101608
YaluVISTA®08052742101561
YaluVISTA®08052742101462
YaluVISTA®08052742101486

1 2

Device characteristics

Implantable

Legacy certificates

Certificate number: CSQ0004231223
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: ISTITUTO SUPERIORE DI SANITA' (0373)
Validity: Oct 6, 2023 → Jan 19, 2028

Certificate number: CVD0002230623
Type: refdata.certificate-mdr-type.technical-documentation
Notified body: ISTITUTO SUPERIORE DI SANITA' (0373)
Validity: May 29, 2023 → Jan 19, 2028

Identity & classification

Basic UDI-DI: 805274210OculadZJ
Device name: Oculade
Device model: Oculade
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Version date: Aug 9, 2023

Manufacturer & authorised representative

Manufacturer

Name: S.A.L.F. S.p.A. Laboratorio Farmacologico
SRN: IT-MF-000010720
Country: Italy
Email: regulatory@salfspa.it
Phone: +39035940097

Variants by status