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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

Syncro Normgelenkfuß… — Class I MDR by Syncro Med…

MD Atlas
Syncro Med Orthopädische Erzeugnisse GmbH

EUDAMED last updated this device on May 29, 2026

Syncro Normgelenkfuß Prothesenfuß, rechts (R), 25 cm, Hell

9120138NORMGELENKFUSS2D

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Syncro Med Orthopädische Erzeugnisse GmbH
UDI-DI code: 09120138014500
Reference / catalog number: SYPRO-NORMG-R-25-H

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View device family (Basic UDI)

Manufacturer information

Organization name: Syncro Med Orthopädische Erzeugnisse GmbH
SRN: AT-MF-000043210
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Austria; available across 2 countries total.

Country	On market since	Until
AustriaPrimary placement	May 29, 2020	Still on market
Germany		Still on market

Device identification

Trade name: Syncro Normgelenkfuß Prothesenfuß, rechts (R), 25 cm, Hell
UDI-DI code: 09120138014500
Basic UDI-DI: 9120138NORMGELENKFUSS2D
Reference / catalog number: SYPRO-NORMG-R-25-H
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: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)09120138014500

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

P090699FOOT PROSTHESES - OTHER

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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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.