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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

BraceID -Double-Cross Back… — Class I MDR by Orthobroker

MD Atlas
Orthobroker

EUDAMED last updated this device on Aug 25, 2022

BraceID -Double-Cross Back Support - Medium

5404020402trunkheadce5B

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Orthobroker
UDI-DI code: 05404020401031
Reference / catalog number: 11-0082-M

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Manufacturer information

Organization name: Orthobroker
SRN: BE-MF-000000331
Manufacturer status: Active

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

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

CW011
Contra Indications • Severe back injuries • Patients known to be sensitised to natural rubber Precautions • The support should fit snugly and comfortably without interfering with respiration. • If discomfort occurs, use should be discontinued and a healthcare professional consulted. • This product contains natural rubber, which may cause allergic reactions • Ensure appropriate wound care procedures are undertaken prior to application over open wounds or infected areas.
CW083
CONTAINS LATEX
CW010
This brace should only be applied in accordance with the instructions mentioned in this manual.

Market distribution

Primary placement in Belgium; available across 2 countries total.

Country	On market since	Until
BelgiumPrimary placement		Still on market
Portugal		Still on market

Device identification

Trade name: BraceID -Double-Cross Back Support - Medium
UDI-DI code: 05404020401031
Basic UDI-DI: 5404020402trunkheadce5B
Reference / catalog number: 11-0082-M
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: Medium

EMDN nomenclature code(s)

Y060318CERVICOTHORACOLUMBOSACRAL SPINE ORTHOSES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

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Serial number
Software identification