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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

PO07173 — Class I MDR by Sahva A/S

MD Atlas
Sahva A/S

EUDAMED last updated this device on May 13, 2026

PO07173

5711433PED001HE

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Sahva A/S
UDI-DI code: 05711433070038
Reference / catalog number: PO07173

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Manufacturer information

Organization name: Sahva A/S
SRN: DK-MF-000051700
Manufacturer status: Active

Related devices

PO071735711433PED001HEOn the market PO071735711433PED001HEOn the market PO071735711433PED001HEOn the market PO071735711433PED001HEOn the market PO071735711433PED001HEOn 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.

Market distribution

Primary placement in Denmark; available across 1 country total.

Country	On market since	Until
DenmarkPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 05711433070038
Basic UDI-DI: 5711433PED001HE
Reference / catalog number: PO07173
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: 70 MU50
Brace, 5-hole configuration

EMDN nomenclature code(s)

Y061215HIP ORTHOSES (INCLUDING ABDUCTION 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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Expiration date
Manufacturing date
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Software identification