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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

PED 102 - 46 — Class I MDR by SUPORTH MED SRL

MD Atlas
SUPORTH MED SRL

EUDAMED last updated this device on May 29, 2026

PED 102 - 46

5944759088SUSTPLANTCARB2P

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SUPORTH MED SRL
UDI-DI code: 05944759088450
Reference / catalog number: PED 102 - 46

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Manufacturer information

Organization name: SUPORTH MED SRL
SRN: RO-MF-000034720
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Romania; available across 1 country total.

Country	On market since	Until
RomaniaPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 05944759088450
Basic UDI-DI: 5944759088SUSTPLANTCARB2P
Reference / catalog number: PED 102 - 46
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: Structura din carbon ultra-ușoară stabilizează glezna și oferă un retur excelent de energie la impact. Reduce oboseala musculară, absoarbe șocurile intense și previne accidentările. Material respirabil, ideal pentru alergare și antrenamente. Mărimea 46
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

EMDN nomenclature code(s)

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

Y061203ORTHOSES, FOOT (INCLUDING INSOLES AND INSERTS)

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

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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.