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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

BD Universal Viral Transport — IVDR Class A IVDR

MD Atlas
Copan Italia S.P.A.

EUDAMED last updated this device on May 21, 2026

BD Universal Viral Transport

80533260BD0260AM0049D

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Copan Italia S.P.A.
UDI-DI code: 18053326009409
Reference / catalog number: 220528

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View device family (Basic UDI)

Manufacturer information

Organization name: Copan Italia S.P.A.
SRN: IT-MF-000022535
Manufacturer status: Active

Related devices

BC+80533260DD0190AM001C5On the market BD FCT80533260CD0140AM0028KOn the market BD Universal Viral Transport80533260BD0260AM0049DOn the market BD Universal Viral Transport80533260BD0260AM0049DOn the market BD Universal Viral Transport80533260BD0260AM0049DOn the market

Certificates

Certificate health across this manufacturer's portfolio.

G10 073936 0018Issued
Quality management systemNotified body: 0123Expiry: Feb 12, 2028
V11 073936 0015Issued
Quality management systemNotified body: 0123Expiry: Apr 18, 2027

Critical warnings

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

CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
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: BD Universal Viral Transport
UDI-DI code: 18053326009409
Basic UDI-DI: 80533260BD0260AM0049D
Reference / catalog number: 220528
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: 3 mL Vial, Flock Regular
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)18053326009409

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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.

W050301020101SAMPLES ANALYSES, PLASTIC TUBES WITH ADDITIVES

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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