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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

NA — IVDR Class A IVDR by DIPRO MEDICAL DEVICES srl

MD Atlas
DIPRO MEDICAL DEVICES srl

EUDAMED last updated this device on Mar 3, 2026

NA

803363889E00184

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: DIPRO MEDICAL DEVICES srl
UDI-DI code: 08033638893654
Reference / catalog number: NA

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View device family (Basic UDI)

Manufacturer information

Organization name: DIPRO MEDICAL DEVICES srl
SRN: IT-MF-000028545
Manufacturer status: Active

Critical warnings

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

CW999
Biological Risk - Infectious Substance
CW999
Biological Substance Category B
CW010
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

Placed on the market in Italy; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 08033638893654
Basic UDI-DI: 803363889E00184
Reference / catalog number: NA
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: Disposable container for the transport of biological samples.
Additional information URL: https://ifu.dipromed.eu/fahnoopoh9aifae4.pdf
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)08033638893654

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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.

W05020180SAMPLES TRANSPORT, CONTAINERS - ACCESSORIES

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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Related devices

NA803363889E00184On the market NA803363889E00184On the market NA803363889E00184On 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.