Катетеры для рентгенэндоваскулярной хирургии: катетер Stingray™ LP / Stingray™ LP Catheter, размер: 3.2 F х 135 см

Страна: Беларусь

Язык: русский

Источник: Министерством здравоохранения Республики (Центр экспертиз и испытаний в здравоохранении)

Доступна с:

Boston Scientific Corporation, СОЕДИНЕННЫЕ ШТАТЫ АМЕРИКИ

класс:

изделия медицинского назначения

Производитель:

Boston Scientific Corporation

Дата Авторизация:

2021-01-28

Характеристики продукта

                                50949163-01
INSTRUCCIONES DE USO
4
MODE D’EMPLOI
6
GEBRAUCHSANWEISUNG
8
ISTRUZIONI PER L’USO
11
GEBRUIKSAANWIJZING
13
INSTRUÇÕES DE UTILIZAÇÃO
15
Boston Scientific (Master Brand DFU Template 5in x 5.25in Global,
90348240AM), DFU, MB, CrossBoss, Global, 50949163-01A
Black (K) ∆E ≤5.0
DIRECTIONS FOR USE
2
CROSSBOSS
™
Catheter
2019-09
2
Boston Scientific (Master Brand DFU Template 5in x 5.25in Global,
90348240AM), DFU, MB, CrossBoss, Global, 50949163-01A
Black (K) ∆E ≤5.0
Black (K) ∆E ≤5.0
ONLY
CAUTION: Federal Law (USA) restricts this device to sale by or on the
order
of a physician.
WARNING
Contents supplied STERILE using a Radiation process. Do not use if
sterile barrier
is damaged. If damage is found, call your Boston Scientific
representative.
For single use only. Do not reuse, reprocess or resterilize. Reuse,
reprocessing
or resterilization may compromise the structural integrity of the
device and/or
lead to device failure which, in turn, may result in patient injury,
illness or
death.
Reuse,
reprocessing
or
resterilization
may
also
create
a
risk
of
contamination of the device and/or cause patient infection or
cross-infection,
including, but not limited to, the transmission of infectious
disease(s) from one
patient to another. Contamination of the device may lead to injury,
illness or
death of the patient.
After use, dispose of product and packaging in accordance with
hospital,
administrative and/or local government policy.
DEVICE DESCRIPTION
The CrossBoss Catheter facilitates the placement and support of a
guidewire
into
discrete
regions
of
the
coronary
vasculature
through
its
central
guidewire lumen. The CrossBoss Catheter contains a rounded distal tip
(1 mm diameter) mounted to a flexible and torqueable proximal shaft.
The
CrossBoss Catheter is packaged with a dedicated torque device
positioned
at its proximal end. The distal end of the catheter is hydrophilic
coated. The
CrossBoss Catheter is compatible with 6F guide catheters with minimum
inner diameter of 0.070 in (1.7 mm), and may 
                                
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