Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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

UDI-DI variants

32 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

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

YaluVISTA®08052742101547
YaluVISTA®08052742101646
YaluVISTA®08052742101769
YaluVISTA®08052742101707
YaluVISTA®08052742101660
YaluVISTA®08052742101745
YaluVISTA®08052742101585

1 2