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21 G x .75 in. BD Vacutainer® Push Button Blood Collection Set with 7 in. tubing and luer adapter is clinically demonstrated to reduce needlestick injuries.
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21 G x .75 in. BD Vacutainer® Push Button Blood Collection Set with 12 in. tubing and no luer adapter is clinically demonstrated to reduce needlestick injuries.
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21 G x .75 in. BD Vacutainer® Push Button Blood Collection Set with 12 in. tubing and luer adapter is clinically demonstrated to reduce needlestick injuries.
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25 G x .75 in. BD Vacutainer® Push Button Blood Collection Set with 12 in. tubing and luer adapter is clinically demonstrated to reduce needlestick injuries.
-
25 G x .75 in. BD Vacutainer® Push Button Blood Collection Set with 12 in. tubing and no luer adapter is clinically demonstrated to reduce needlestick injuries.
-
23 G x .75 in. BD Vacutainer® Push Button Blood Collection Set with 12 in. tubing and no luer adapter is clinically demonstrated to reduce needlestick injuries.
-
23 G x .75 in. BD Vacutainer® Push Button Blood Collection Set with 7 in. tubing and luer adapter is clinically demonstrated to reduce needlestick injuries.
-
25 G x .75 in. BD Vacutainer® Push Button Blood Collection Set with 7 in. tubing and luer adapter is clinically demonstrated to reduce needlestick injuries.
-
23 G x .75 in. BD Vacutainer® Push Button Blood Collection Set with 12 in. tubing and luer adapter is clinically demonstrated to reduce needlestick injuries.
true
- Overzicht
- Products & Accessories
- EIFU & Bronnen
false
Eenhandige activering
Met de eenhandige veiligheidsactivering van de push button kunt u het veiligheidsmechanisme activeren en tegelijkertijd de patiënt en de venapunctielocatie blijven observeren.
Efficiëntie
Voorgemonteerde houders elimineren stappen in het flebotomieproces.
false
true
false
true
Houd er rekening mee dat mogelijk niet alle producten, diensten of functies van producten en diensten beschikbaar zijn in uw regio. Neem contact op met uw lokale BD vertegenwoordiger.
Dit medische hulpmiddel heeft een CE-markering in navolging van de Europese Richtlijn Medische Hulpmiddelen 93/42/EEG en is CE-gecertificeerd door NSAI - National Standards Authority of Ireland (Nummer aangemelde instantie = 0050)
BD-113313
true