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Organization name
UDI-DI code
Reference / catalog number

5999881214413 — Class I MDR by Motto-Elektro…

MD Atlas
Motto-Elektro Kereskedelmi és Szolgáltató Korlátolt Felelősségű Társaság

EUDAMED last updated this device on Feb 15, 2022

5999881214413

5999881214819KR

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Motto-Elektro Kereskedelmi és Szolgáltató Korlátolt Felelősségű Társaság
UDI-DI code: 05999881214413
Reference / catalog number: 5999881214413

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Manufacturer information

Organization name: Motto-Elektro Kereskedelmi és Szolgáltató Korlátolt Felelősségű Társaság
SRN: HU-MF-000003865
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW011
Prodotto per uso esterno! Non utilizzare su cute lesa! Non sterile. Prima dell’uso leggere attentamente le avvertenze e le modalità d’uso. L’adesivo contiene LATEX, che può provocare una reazione allergica in chi ne è sensibile. Non sono disponibili informazioni sufficienti riguardo l’uso del cerotto per bambini e madri in gravidanza e in allattamento.

Market distribution

Primary placement in Hungary; available across 2 countries total.

Country	On market since	Until
HungaryPrimary placement	Jan 1, 1982	Still on market
Italy	May 6, 2014	Still on market

Device identification

Trade name: not provided
UDI-DI code: 05999881214413
Basic UDI-DI: 5999881214819KR
Reference / catalog number: 5999881214413
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: 2
Additional product description: Cerotto analgesico senza medicinali. È utile come coadiuvante per apportare sollievo in caso di dolore cronico articolare e muscolare.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 10–25 MU82

EMDN nomenclature code(s)

M0599MEDICAL PLASTERS - 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

Related devices

59998812148265999881214826KNOn the market 59998812148335999881214826KNOn the market 59998812148195999881214819KROn 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.