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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

527002 — Class I MDR by Brunngård Group AB

MD Atlas
Brunngård Group AB

EUDAMED last updated this device on May 27, 2026

527002

739327452700273

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Brunngård Group AB
UDI-DI code: 739327452700273
Reference / catalog number: 527002

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View device family (Basic UDI)

Manufacturer information

Organization name: Brunngård Group AB
SRN: SE-MF-000055319
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Sweden; available across 1 country total.

Country	On market since	Until
SwedenPrimary placement	Oct 10, 2022	Dec 30, 2030

Device identification

Trade name: not provided
UDI-DI code: 739327452700273
Basic UDI-DI: 739327452700273
Reference / catalog number: 527002
Issuing entity: HIBCC

Classification

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

Device details

Quantity: 2
Additional product description: Elastiskt nylon-skydd som tryckavlastar och lindrar besvär orsakade av Hallux Valgus. Mjukt och smidigt skydd med en insydd kudde av silikongel som skyddar stortåleden mot tryck. Sitter stadigt på foten och är enkel att sätta på och ta av. Säljs i par. Universal vänster/höger. Kan handtvättas.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

739327452700273

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Y06120601PASSIVE ANKLE-FOOT 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

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Related devices

52700173932745270016ZOn the market 527003739327452700375On the market 527004739327452700477On the market

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.