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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

70071, 70373 — Class I MDD by CANFIELD SCIENTIFIC SRL

MD Atlas
CANFIELD SCIENTIFIC SRL

EUDAMED last updated this device on Apr 29, 2026

70071, 70373

B-80531722200134

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: CANFIELD SCIENTIFIC SRL
UDI-DI code: 80531722200134
Reference / catalog number: 70071, 70373

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View device family (Basic UDI)

Manufacturer information

Organization name: CANFIELD SCIENTIFIC SRL
SRN: IT-MF-000034524
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW273
Unplug device before maintenance operations

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Oct 18, 2010	Still on market

Device identification

Trade name: not provided
UDI-DI code: 80531722200134
Basic UDI-DI: B-80531722200134
Reference / catalog number: 70071, 70373
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Digital video dermatoscope and capillaroscope
Additional information URL: https://www.canfieldsci.com/imaging-systems/vidix/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)80531722200134

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z12040107CAPILLARISCOPES
Z12040118VIDEO DERMATOSCOPES

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

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Related devices

70191B-80531722200202On the market VTRACK805317222VTRACKGKOn the market VIDIX805317222VIDIXAQOn 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.