BrownGuard 2000 long wrist orthosis type 04

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: • signs of mechanical damage appear (replace the orthosis with a new one) • you observe deterioration of your health condition that could be related to the use of the long wrist orthosis – in such a case, consult your attending physician Contraindications: • disease or skin injury in the wrist area • acute weeping skin manifestations • hypersensitivity to the materials used • lymph drainage disorders and non-specific soft tissue oedema in the wrist area • limb sensitivity disorders, peripheral neuropathy

Primary placement in Czechia; available across 1 country total.

Trade name

BrownGuard 2000 long wrist orthosis type 04

UDI-DI code

08590072959280

Basic UDI-DI

85900722025073J

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 designed to support the wrist during post-traumatic and post-operative therapy, in case of flabby muscles, inflammation, or injury to wrist ligaments and tendons and to prevent swelling.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• S
• left
• 9999

• Y060609WRIST (FOREARM) ORTHOSES

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