Diafit PREMIUM medical socks

Organization name

ARIES, a.s.

SRN

CZ-MF-000047385

Manufacturer status

Active

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

• CW999

  When not to use: Discontinue use of the medical device immediately if: • There are signs of mechanical damage – replace with new device • You notice a deterioration in your health that may be associated with the use of the medical device – consult your doctor in such case Contraindications: • Acute weeping skin manifestations • Irritated or otherwise broken skin • Hypersensitivity to materials used

Primary placement in Czechia; available across 1 country total.

Placed on the market in Czechia; per-country availability dates not published.

Trade name

Diafit PREMIUM medical socks

UDI-DI code

08590072928828

Basic UDI-DI

85900722019043R

Reference / catalog number

NA

Issuing entity

GS1

Risk category

Class I

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

The medical device intended for diabetics and patients with sensitive skin of the lower limbs.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• 39-42
• 8002

• Y090699DEVICES FOR BODY PROTECTION - OTHER

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