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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

8029408130623 — Class I MDD by UNIFARCO SpA

MD Atlas
UNIFARCO SpA

EUDAMED last updated this device on Jan 8, 2026

8029408130623

B-FPGAFT10TFU

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: UNIFARCO SpA
UDI-DI code: D-FPGAFT10TFU
Reference / catalog number: 8029408130623

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View device family (Basic UDI)

Manufacturer information

Organization name: UNIFARCO SpA
SRN: IT-MF-000013304
Manufacturer status: Active

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Critical warnings

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

CW275
Nach dem derzeitigen Kenntnisstand kann das Produkt auch während der Schwangerschaft und Stillzeit angewendet werden. Dennoch sollte stets der behandelnde Arzt zurate gezogen werden
CW135
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Germany; available across 2 countries total.

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

Device identification

Trade name: not provided
UDI-DI code: D-FPGAFT10TFU
Basic UDI-DI: B-FPGAFT10TFU
Reference / catalog number: 8029408130623
Issuing entity: EUDAMED

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

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

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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

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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.