20DM

Organization name

ITALRES SRL

SRN

IT-MF-000029584

Manufacturer status

Active

1 warning recorded — scroll inside the panel to see all entries.

• CW999

  Do not use during pregnancy, if you have implanted electrical devices or epilepsy. If you experience any irritation, itching or marking of the skin or any other adverse symptoms from using this device, discontinue use immediately.

Primary placement in Denmark; available across 4 countries total.

Trade name

not provided

UDI-DI code

08053848210065

Basic UDI-DI

80538482120DM6E

Reference / catalog number

20DM

Issuing entity

GS1

Risk category

Class IIa

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

Compact, fast-working and taking just 30 seconds, use Paingone Plus in the home, the office, or during activity. It can even be applied through light clothing, so you always have effective relief available whenever you need it.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• Z12062899NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER

Certificate health across this manufacturer's portfolio.