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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

60434351 — Class I MDR by BBS S.r.l.

MD Atlas
BBS S.r.l.

EUDAMED last updated this device on May 20, 2026

60434351

++G197CertiLabelAY

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BBS S.r.l.
UDI-DI code: +G197604343510
Reference / catalog number: 60434351

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View device family (Basic UDI)

Manufacturer information

Organization name: BBS S.r.l.
SRN: IT-MF-000007274
Manufacturer status: Active

Related devices

60434348++G197CertiLabelAYOn the market 60434349++G197CertiLabelAYOn the market 60434357++G197CertiLabelAYOn the market 60434365++G197CertiLabelAYOn the market 60434352++G197CertiLabelAYOn the market

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: +G197604343510
Basic UDI-DI: ++G197CertiLabelAY
Reference / catalog number: 60434351
Issuing entity: HIBCC

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 7500
Additional product description: Etichetta Triplex 76x88,5 mm pretagliata con adesivo certificato + ribbon
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

+G197604343510

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.

B0180BLOOD BAGS AND KITS - 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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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.