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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

DAMO — Class I MDR by Murphil srl

MD Atlas
Murphil srl

EUDAMED last updated this device on May 8, 2026

DAMO

805621582dosex3Z

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Murphil srl
UDI-DI code: 80562158200030
Reference / catalog number: DAMO

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View device family (Basic UDI)

Manufacturer information

Organization name: Murphil srl
SRN: IT-MF-000044291
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	May 8, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 80562158200030
Basic UDI-DI: 805621582dosex3Z
Reference / catalog number: DAMO
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: DAMO is qualified as a medical device under the MDR, as defined in the MDR, Article 1.4, Article 2 (1), as it is an instrument intended by the manufacturer to be used for humans to measure the activity of radiopharmaceuticals used for the diagnosis or treatment of diseases. The radiopharmaceutical is measured directly in a syringe or vial before administration to patients.
Additional information URL: https://www.murphil.eu/
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)80562158200030

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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.

Z11029005AUTOMATIC DOSE CALIBRATORS

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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Related devices

DAMO S20805621582dosex3ZOn the market DAMO S8M805621582dosex3ZOn 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.