BrownGuard 700 back orthosis type 02

Organization name

ARIES, a.s.

SRN

CZ-MF-000047385

Manufacturer status

Active

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• CW999

  When not to use: Immediately discontinue use of the medical device if you observe a deterioration in your health that may be related to its use –⁠ in such a case, consult with your treating physician. Contraindications: • Skin diseases or injuries in the lumbar and thoracic spine • Acute weeping skin manifestations • Hypersensitivity to materials used • Lymphatic drainage disorders and non-specific soft tissue oedema in the lumbar and thoracic spin area

Primary placement in Czechia; available across 1 country total.

Trade name

BrownGuard 700 back orthosis type 02

UDI-DI code

08590072917921

Basic UDI-DI

85900722024183J

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 is designed to support the lumbar and thoracic spine during post-trauma and post-surgical therapy, prevent swelling and serve as support in cases of weakness, inflammation or injury of ligaments and tendons in the lumbar and thoracic areas. This brace is suitable as a therapeutic or preventive device.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• L
• thoraco-lumbar, reinforced
• 9999

• Y060306THORACOLUMBAR ORTHOSES

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