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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

aabbbcccXd0e — Class IIa MDR by Bosco Ottica srl

MD Atlas
Bosco Ottica srl

EUDAMED last updated this device on May 27, 2025

aabbbcccXd0e

++G294FIBRAOTTICAG4

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Bosco Ottica srl
UDI-DI code: G2942FIBRE0
Reference / catalog number: aabbbcccXd0e

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View device family (Basic UDI)

Manufacturer information

Organization name: Bosco Ottica srl
SRN: IT-MF-000029714
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: G2942FIBRE0
Basic UDI-DI: ++G294FIBRAOTTICAG4
Reference / catalog number: aabbbcccXd0e
Issuing entity: HIBCC

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: Fibre ottiche, utilizzate per il trasporto della luce laser da un dispositivo medico attivo ad un punto di interesse. Sono disponibili in diverse varianti, che differiscono per materiali impiegati, connettori (FC, SMA standard, SMA Free Standing, ferule), diametro e lunghezza della fibra. Possono essere anche rivestite da una guaina in silicone o C-Flex
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

G2942FIBRE0

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

EMDN nomenclature code(s)

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

Z12011080LASER SURGERY INSTRUMENTS - HARDWARE ACCESSORIES

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

This device is not currently linked to any other device.

Certificates

Certificate health across this manufacturer's portfolio.

IT341234Issued
Quality management systemNotified body: 1370Expiry: Mar 27, 2030