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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

SMOKE FILTER — Class I MDR by BIOGYN SRL

MD Atlas
BIOGYN SRL

EUDAMED last updated this device on Apr 29, 2026

SMOKE FILTER

805697735003JN

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BIOGYN SRL
UDI-DI code: 18056977352054
Reference / catalog number: SFF1 N120

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Manufacturer information

Organization name: BIOGYN SRL
SRN: IT-MF-000033403
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Dec 2, 2000	Dec 30, 2999

Device identification

Trade name: SMOKE FILTER
UDI-DI code: 18056977352054
Basic UDI-DI: 805697735003JN
Reference / catalog number: SFF1 N120
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: 5
Additional product description: FILTRO FUMI AI CARBONI ATTIVI, ANTIBATTERICO E ANTIVIRALE
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

UDI-DI DataMatrix

Encoded

(01)18056977352054

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

K02010107SMOKE EVACUATION SYSTEMS

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

CLAMP CUTTER805697735008JYOn the market EBR1 N25805697735000JGOn the market ENDOBRUSH805697735000JGOn the market PLASTIC SPATULA805697735000JGOn the market SMOKE FILTER805697735003JNOn 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.