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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

DualVis — Class III MDD by MDT Int'l SA

MD Atlas
MDT Int'l SA

EUDAMED last updated this device on Nov 1, 2023

DualVis

B-07640153260031

On the marketClass III

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: MDT Int'l SA
UDI-DI code: 07640153260031
Reference / catalog number: M301D002T

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Manufacturer information

Organization name: MDT Int'l SA
SRN: CH-MF-000028146
Manufacturer status: Active

Related devices

GAFB-07640153260093On the market RenehaVisB-07640153260048On the market SportVisB-07640153260321On the market SportVisB-07640153260024On the market TendoVisB-07640153260079On 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.

Critical warnings

5 warnings recorded — scroll inside the panel to see all entries.

CW011
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Türkiye; available across 2 countries total.

Country	On market since	Until
TürkiyePrimary placement		Still on market
Austria		Still on market

Device identification

Trade name: DualVis
UDI-DI code: 07640153260031
Basic UDI-DI: B-07640153260031
Reference / catalog number: M301D002T
Issuing entity: GS1

Classification

Risk category: Class III
Applicable legislation: MDD [Directive 93/42/EEC 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)

P9099IMPLANTABLE PROSTHETIC 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