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7 DE/AT/CH
Bevollmächtigter EU-Repräsentant für
Hersteller von Medizinprodukten
Anwendungsteil Typ BF
Seriennummer
0123
Die CE-Kennzeichnung bescheinigt die
Konformität mit den grundlegenden
Anforderungen der Richtlinie 93/42/EEC
für Medizinprodukte.
Umweltschäden durch falsche Entsorgung
der Batterien!
IP21
Gerät geschützt gegen Fremdkörper ≥12,5 mm
und gegen senkrechtes Tropfwasser
21
PAP
Verpackung und Blutdruckmessgerät
umweltgerecht entsorgen!
Datenübertragung per Bluetooth® low
energy technology
7


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