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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

INBRUSH — Class I MDR by BIHOS S.r.l.

MD Atlas
BIHOS S.r.l.

EUDAMED last updated this device on May 21, 2026

INBRUSH

8033480R0105802K

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BIHOS S.r.l.
UDI-DI code: 08033480009074
Reference / catalog number: BSP10000M

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View device family (Basic UDI)

Manufacturer information

Organization name: BIHOS S.r.l.
SRN: IT-MF-000028025
Manufacturer status: Active

Related devices

BIHEX8033480G020401U5On the market BIOLUB8033480V9099P7On the market BIOMILK8033480MILK2EOn the market BIOMILK8033480MILK2EOn the market INBRUSH8033480R0105802KOn 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

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		Still on market

Device identification

Trade name: INBRUSH
UDI-DI code: 08033480009074
Basic UDI-DI: 8033480R0105802K
Reference / catalog number: BSP10000M
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: 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

UDI-DI DataMatrix

Encoded

(01)08033480009074

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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.

R01058099TRACHEOSTOMY AND LARYNGECTOMY CANNULAS - VARIOUS 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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