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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

Lymed Skin — Class I MDR by Lymed Oy

MD Atlas
Lymed Oy

EUDAMED last updated this device on Apr 29, 2022

Lymed Skin

06438472800103NQ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Lymed Oy
UDI-DI code: 06438472800103
Reference / catalog number: STPR

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Manufacturer information

Organization name: Lymed Oy
SRN: FI-MF-000015063
Manufacturer status: Active

Related devices

Lymed Compression06438472800202NTOn the market Lymed Interim & Light06438472800400NZOn the market Lymed Post-operation06438472800509PQOn the market Lymed Sense06438472800301NWOn 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 Finland; available across 1 country total.

Placed on the market in Finland; per-country availability dates not published.

Device identification

Trade name: Lymed Skin
UDI-DI code: 06438472800103
Basic UDI-DI: 06438472800103NQ
Reference / catalog number: STPR
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: Pressure garment
Additional information URL: https://www.lymed.fi/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M030499ELASTIC BANDAGES, SUPPORT AND COMPRESSION - 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification