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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

DW100 — Class I MDR by DMED DI D IMPRIMA ANGELO

MD Atlas
DMED DI D IMPRIMA ANGELO

EUDAMED last updated this device on Jun 5, 2025

DW100

805517623DW1004T

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: DMED DI D IMPRIMA ANGELO
UDI-DI code: 80551762300984
Reference / catalog number: DW100

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View device family (Basic UDI)

Manufacturer information

Organization name: DMED DI D IMPRIMA ANGELO
SRN: IT-MF-000032812
Manufacturer status: Active

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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.

Critical warnings

No critical warnings reported for this device.

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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: 80551762300984
Basic UDI-DI: 805517623DW1004T
Reference / catalog number: DW100
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: Decontamination system installed in an existing or new counter sink.
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)80551762300984

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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.

Z12011301CLEANING AND DISINFECTION EQUIPMENT
Z12011306CLEANING AND DECONTAMINATION SYSTEMS FOR GENERAL AND MULTIDISCIPLINARY SURGERY INSTRUMENTS

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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