Painaway

Organization name

ITALRES SRL

SRN

IT-MF-000029584

Manufacturer status

Active

Certificate health across this manufacturer's portfolio.

2 warnings recorded — scroll inside the panel to see all entries.

• CW010

  Caution: keep out of the reach of children, read the instructions before use
• CW999

  Do not use: - If you have a pacemaker or other implanted electrical device - If you have epilepsy - During pregnancy - 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 1 country total.

Trade name

Painaway

UDI-DI code

08053848210027

Basic UDI-DI

80538482110DM,30DMX8

Reference / catalog number

30DM

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

An effective way to soothe joint and muscle pain without using medication. PainAway is a 100% drug free device. TENS device for the symptomatic temporary relief of acute and chronic musculoskeletal pain (excluding pain resulting from bone fractures). • Temporary relief of pain associated with osteoarthritis • Compact, light, easy to use and can be used over light clothes • Works without batteries, electrodes or wires • Operating life: 24 months

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