PF-0001

Organization name

Stimuli Technology

SRN

FR-MF-000002429

Manufacturer status

Active

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

• CW010

  EUDAMED did not publish a description for this code.
• CW030

  If you have a pacemaker, defibrillator, or any other electronic implant, as this could cause an electric shock, interference, burns, or cause your pacemaker to malfunction; if you have a metal implant near the stimulated area, as this could result in burns or cause interference with Tensi+; if you have ankle joint problems, swollen ankles or a dermatological condition or damaged skin in the area where the electrodes are to be placed; if you are pregnant; if you have a cognitive impairment. If in doubt, ask your doctor.
• CW007

  Do not use the product if either the product or packaging is damaged.

Primary placement in France; available across 4 countries total.

Trade name

not provided

UDI-DI code

03760316090009

Basic UDI-DI

376031609PF007X

Reference / catalog number

PF-0001

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

—

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

• N010103BIPOLAR NERVOUS ELECTROSTIMULATORS, BATTERY-POWERED

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