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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

"Easy Tainer Max®" Polyethylene… — IVDR Class A IVDR

MD Atlas
SYNTESYS S.R.L.

EUDAMED last updated this device on Mar 12, 2026

"Easy Tainer Max®" Polyethylene bottle, graduated for 24h urine collection, 3L, for photosensible analysis with vacuum system

805414149CONTURINANZ

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: SYNTESYS S.R.L.
UDI-DI code: 08054141490710
Reference / catalog number: 390599

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View device family (Basic UDI)

Manufacturer information

Organization name: SYNTESYS S.R.L.
SRN: IT-MF-000027856
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.
CW030
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: "Easy Tainer Max®" Polyethylene bottle, graduated for 24h urine collection, 3L, for photosensible analysis with vacuum system
UDI-DI code: 08054141490710
Basic UDI-DI: 805414149CONTURINANZ
Reference / catalog number: 390599
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: —
Additional information URL: https://www.syntesys.it/appwp/wp-content/uploads/2025/06/IFU-IVDR-2017-746-20250606.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)08054141490710

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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.

W05010203URINE COLLECTION, CONTAINERS

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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Related devices

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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.