Paingone One

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 if you have a pacemaker or other implanted electrical device, if you have epilepsy, during pregnancy, or 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 Germany; available across 4 countries total.

Trade name

Paingone One

UDI-DI code

08053848210003

Basic UDI-DI

80538482110DM,30DMX8

Reference / catalog number

10DM

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

Paingone One is the portable pain relief device that can be used anywhere and anytime, whenever you need it, for temporary relief of musculoskeletal pain. It delivers a controlled electrical frequency straight to the point of pain. This clinically proven therapy can provide prolonged and often instant pain relief. Paingone One takes just one minute to use and can be applied through clothing. With almost 2 million sold worldwide, its success speaks for itself.

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.