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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 S8M — Class I MDR by Murphil srl

MD Atlas
Murphil srl

EUDAMED last updated this device on May 22, 2026

DAMO S8M

805621582dosex3Z

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Murphil srl
UDI-DI code: 80562158200276
Reference / catalog number: DAMO S8M

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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: 80562158200276
Basic UDI-DI: 805621582dosex3Z
Reference / catalog number: DAMO S8M
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 MDR, according to the definition of MDR, Article 1.4, Article 2 (1), since it is an instrument intended by the manufacturer to be used for human beings to measure the activity of radiopharmaceuticals used for diagnosis or treatment of disease. The pharmaceutical is measured directly in a syringe or vial prior to 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)80562158200276

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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 DAMO805621582dosex3ZOn 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.