VBM-PRO-LOL

Organization name

Techno Concept

SRN

FR-MF-000002558

Manufacturer status

Active

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

• CW999

  Without medical advice from the practitioner responsible of the patient care, the use of VIBRAMOOV range is contraindicated for: - Patients with phlebitis or risk of thrombosis - Patients with epilepsy - Patients with fragile skin.

Primary placement in France; available across 3 countries total.

Trade name

not provided

UDI-DI code

03701523700015

Basic UDI-DI

37015237VIBRAMOOVES

Reference / catalog number

VBM-PRO-LOL

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.

• Z12069099VARIOUS PHYSIOTHERAPY AND REHABILITATION INSTRUMENTS - OTHER

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

Certificate health across this manufacturer's portfolio.