Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ 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.

Organization name
UDI-DI code
Reference / catalog number

70 — Class I MDR by DIAGONAL d.o.o. za…

MD Atlas
DIAGONAL d.o.o. za trgovinu i usluge

EUDAMED last updated this device on Jun 6, 2025

70

385889580ORGLEN167SVPHXC

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: DIAGONAL d.o.o. za trgovinu i usluge
UDI-DI code: 03858895801113
Reference / catalog number: 70

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?

Manufacturer information

Organization name: DIAGONAL d.o.o. za trgovinu i usluge
SRN: HR-MF-000047457
Manufacturer status: Active

Related devices

001385889580ORGLEN167SVCLWDOn the market 002385889580ORGLEN167PRCLV4On the market 003385889580ORGLEN150SVCLTKOn the market 004385889580ORGLEN153SVCLULOn the market 005385889580ORGLEN156SVCLVMOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Market distribution

Primary placement in Croatia; available across 1 country total.

Placed on the market in Croatia; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 03858895801113
Basic UDI-DI: 385889580ORGLEN167SVPHXC
Reference / catalog number: 70
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q0210010101MONOFOCAL ORGANIC OPHTHALMIC LENSES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification