BrownGuard 100 arm sling type 02

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: • You observe a deterioration in your health that may be related to the use of the sling –⁠ in such a case, consult with your treating physician • Signs of mechanical damage appear (replace the sling with a new one) Contraindications: • Injury or scarring at the point of contact with the sling • Skin diseases at the point of contact with the sling (e.g. wet skin manifestations, eczema, ...) • Hypersensitivity to the materials used in the sling

Primary placement in Czechia; available across 1 country total.

Trade name

BrownGuard 100 arm sling type 02

UDI-DI code

08590072876846

Basic UDI-DI

85900722024073D

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 sling designed to ensure the ideal position of the arm for patients with arm impairment with central or peripheral paresis and post-traumatic conditions.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• L
• double-sided
• 9999

• Y090612ARM AND ELBOW PROTECTIONS

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