<H1> Where to find us globally. </H1> |
<H1> Radio Equipment Directive Declaration of Conformity </H1> |
<H1> Radio Equipment Directive Declaration of Conformity </H1> |
<H1> Radio Equipment Directive Declaration of Conformity </H1> |
<H1> Radio Equipment Directive Declaration of Conformity </H1> |
<H1> Radio Equipment Directive Declaration of Conformity </H1> |
<H1> Radio Equipment Directive Declaration of Conformity </H1> |
<H1> Radio Equipment Directive Declaration of Conformity </H1> |
<H1> Radio Equipment Directive Declaration of Conformity </H1> |
<H1> Radio Equipment Directive Declaration of Conformity </H1> |
<H1> Radio Equipment Directive Declaration of Conformity </H1> |
<H1> Radio Equipment Directive Declaration of Conformity </H1> |
<H1> Radio Equipment Directive Declaration of Conformity </H1> |
<H1> Declaration of Conformity </H1> |
<H2> Canada </H2> |
<H2> Europe </H2> |
<H2> Middle East </H2> |
<H2> Oceania </H2> |
<H2> The Netherlands </H2> |
<H2> USA </H2> |
<H2> 1. Legal manufacturer details </H2> |
<H2> 2. Authorized Representative: </H2> |
<H2> 3. Declaration: </H2> |
<H2> 4. description of the Device </H2> |
<H2> 5. Declaration made on behalf of legal manufacturer by: </H2> |
<H2> 1. Podrobnosti o výrobci </H2> |
<H2> 2. Autorizovaný zástupce: </H2> |
<H2> 3. Prohlášení: </H2> |
<H2> 4. Popis prostředku </H2> |
<H2> 5. Prohlášení jménem výrobce vydal/a: </H2> |
<H2> 1. Oplysninger om juridisk producent </H2> |
<H2> 2. Autoriseret repræsentante: </H2> |
<H2> 3. Erklæring: </H2> |
<H2> 4. Beskrivelse af enheden </H2> |
<H2> 5. Erklærering på vegne af juridisk producent: </H2> |
<H2> 1. Gegevens Fabrikant: </H2> |
<H2> 2. Gemachtigde: </H2> |
<H2> 3. Verklaring: </H2> |
<H2> 4. Beschrijving van de Apparatuur </H2> |
<H2> 5. Verldaring gedaan in naam van de fabrikant door: </H2> |
<H2> 1. Lainmukaiset valmistajan tiedot </H2> |
<H2> 2. Valtuutettu edustaja: </H2> |
<H2> 3. Vakuutuslausunto: </H2> |
<H2> 4. Laitteen kuvaus </H2> |
<H2> 5. Vakuutuksen on tehnyt laillisen valmistajan puolesta: </H2> |
<H2> 1. Informations détaillées concernant le fabricant légal </H2> |
<H2> 2. Représentant autorisé : </H2> |
<H2> 3. Déclaration : </H2> |
<H2> 4. description du dispositif </H2> |
<H2> 5. Déclaration faite au nom du fabricant légal par: </H2> |
<H2> 1. Legaler Hersteller </H2> |
<H2> 2. Bevollmächtigter Vertreter in der Europäischen Union: </H2> |
<H2> 3. Erklärung: </H2> |
<H2> 4. Produktbeschreibung </H2> |
<H2> 5. Im namen des legalen Herstellers abgegebene Erklärung: </H2> |
<H2> 1.A gyártó adatai </H2> |
<H2> 2. Meghatalmazott képviselő: </H2> |
<H2> 3. Nyilatkozat: </H2> |
<H2> 4.Az eszköz ismertetése </H2> |
<H2> 5. Nyilatkozattevő a gyártó nevében </H2> |
<H2> 1. Dati legali del produttore </H2> |
<H2> 2. Rappresentante autorizzato: </H2> |
<H2> 3. Dichiarazione: </H2> |
<H2> 4. Descrizione del dispositivo </H2> |
<H2> 5. Dichiarazione resa per conto del legale produttore da: </H2> |
<H2> 1. Datos legales del fabricante </H2> |
<H2> 2. Representante autorizado: </H2> |
<H2> 3. Declaración: </H2> |
<H2> 4. Descripción del dispositivo </H2> |
<H2> 5. Declaración realizada de parte del fabricante legal por: </H2> |
<H2> 1. Information om juridisk tillverkare </H2> |
<H2> 2. Auktoriserad representant: </H2> |
<H2> 3. Försäkran: </H2> |
<H2> 4. Beskrivning av enheten </H2> |
<H2> 5. Försäkran gjord på uppdrag av juridisk tillverkare av: </H2> |
<H2> 1. Detaljer om produsenten </H2> |
<H2> 2. Autorisert representant: </H2> |
<H2> 3. Erldæring: </H2> |
<H2> 4. Beskrivelse av enheten </H2> |
<H2> 5. Erldæring utstedt på vegne av produsenten av: </H2> |
<H2> Manufacturer: </H2> |
<H2> European Representative: (Effective January 1, 2013) </H2> |
<H2> Product: </H2> |
<H2> Medical Device Classification: </H2> |
<H2> Device Accessory Classification: </H2> |
<H2> DIRECTIVES </H2> |
<H2> Notified Body: </H2> |
<H2> Certificates: </H2> |
<H3> Austria </H3> |
<H3> Czech Republic </H3> |
<H3> Denmark </H3> |
<H3> Finland </H3> |
<H3> France </H3> |
<H3> Germany </H3> |
<H3> Hungary </H3> |
<H3> Ireland </H3> |
<H3> Italy </H3> |
<H3> Norway </H3> |
<H3> Spain </H3> |
<H3> Sweden </H3> |
<H3> United Kingdom </H3> |
<H3> Israel </H3> |
<H3> Middle East & Africa </H3> |
<H3> Saudi Arabia </H3> |
<H3> Australia </H3> |
<H3> New Zealand </H3> |
<H3> Canada </H3> |
<H3> Europe </H3> |
<H3> Middle East </H3> |
<H3> Oceania </H3> |
<H3> The Netherlands </H3> |
<H3> USA </H3> |
<H3> Choose language </H3> |
<H3> General Applicable Directive(s): </H3> |
<H3> Specific Applicable Directive(s): </H3> |
<H3> Product details: </H3> |
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Cost and overhead previously rendered this semi-public form of communication unfeasible.
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