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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

527003 — Class I MDR by Brunngård Group AB

MD Atlas
Brunngård Group AB

EUDAMED last updated this device on May 27, 2026

527003

739327452700375

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Brunngård Group AB
UDI-DI code: 739327452700375
Reference / catalog number: 527003

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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: 739327452700375
Basic UDI-DI: 739327452700375
Reference / catalog number: 527003
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: 1
Additional product description: Mjukt tubformat tåskydd med insida av silikon som skyddar, lindrar smärta och återfuktar huden. Lindrar besvär i samband med Hallux Vagus, hammartå, skav eller blåsor. Fungerar utmärkt även på fingrarna. Mått: 200 mm, ø 20 mm. Klipps till önskad längd. 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

739327452700375

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 527002739327452700273On 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.