BraceID-PRESERVER Knee Brace-XLR

Organization name

Orthobroker

SRN

BE-MF-000000331

Manufacturer status

Active

4 warnings recorded — scroll inside the panel to see all entries.

• CW999

  The product should only be used in case of a medical indication or when prescribed by a physician. It should also be applied by a competent orthopaedic technician. This person has also the responsibility to provide the patient accurate information about correct and safe use, according his/her individual needs. The patient should under no circumstances make any change or adjustment to the brace without the consent of physician or orthopaedic technician(i.e. application or removal of hinge wedges).
• CW011

  • Don’t apply the straps too tight that it interferes with circulation or that nerves experience too much compression. • If unusual swelling, skin discoloration or discomfort occurs, use should be discontinued and a healthcare professional consulted. • In case you have doubts about the application of the product, you should contact an orthopaedic specialist (doctor or technician).
• CW262

  • The product is intended for single patient use.
• CW010

  • This brace should only be applied in accordance with the instructions mentioned in the manual

Primary placement in Belgium; available across 1 country total.

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

Trade name

BraceID-PRESERVER Knee Brace-XLR

UDI-DI code

05404020402144

Basic UDI-DI

5404020402kneehipFJ

Reference / catalog number

12-0025-XLR

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

—

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• XLR= Xlarge Right

• Y061209KNEE ORTHOSES

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