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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

14981 — Class I MDR by Sahva A/S

MD Atlas
Sahva A/S

EUDAMED last updated this device on May 13, 2026

14981

5711433ORTHO0013Y

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Sahva A/S
UDI-DI code: 05711433002503
Reference / catalog number: 14981

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Manufacturer information

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

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: 05711433002503
Basic UDI-DI: 5711433ORTHO0013Y
Reference / catalog number: 14981
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: 50 MU10
Left

EMDN nomenclature code(s)

Y062409TRANSTIBIAL PROSTHESES (FOR AMPUTATION UNDER KNEE)
Y062412KNEE DISARTICULATION PROSTHESES
Y062415TRANSFEMORAL PROSTHESES (FOR AMPUTATION ABOVE KNEE)

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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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.