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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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Organization name
UDI-DI code
Reference / catalog number

SiVIEW EXAM — Class IIa MDR by SiVIEW

MD Atlas
SiVIEW

EUDAMED last updated this device on Sep 16, 2025

SiVIEW EXAM

3770022197SIVIEWEXAMPA

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SiVIEW
UDI-DI code: 03770022197015
Reference / catalog number: SiVIEW EXAM

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Manufacturer information

Organization name: SiVIEW
SRN: FR-MF-000007298
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Jun 19, 2019	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03770022197015
Basic UDI-DI: 3770022197SIVIEWEXAMPA
Reference / catalog number: SiVIEW EXAM
Issuing entity: GS1

Classification

Risk category: Class IIa
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)

Q0299OPHTHALMIC DEVICES - OTHER

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

Related devices

BX23770022197BX23JOn the market VC3770022197SCV6EOn the market DG-0043770022197BX23JOn the market DG-0033770022197BX23JOn the market DG-0023770022197BX23JOn the market

Certificates

Certificate health across this manufacturer's portfolio.

283/MDRIssued
Quality management systemNotified body: 0051Expiry: Apr 29, 2030