Принадлежности к кардиоресинхронизирующим кардиостимуляторам и дефибрилляторам: катетер направляющий ACUITY PRO/ACUITY PRO Guide Catheter (модели: 8100, 8101, 8102, 8103, 8104, 8105, 8106, 8107, 8108, 8109, 8110, 8111, 8112, 8113, 8114, 8115, 8116, 8117, 8118, 8119)

Страна: Білорусь

мова: російська

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

Доступна з:

Boston Scientific Corporation, СОЕДИНЕННЫЕ ШТАТЫ АМЕРИКИ

Клас:

изделия медицинского назначения

Виробник:

Boston Scientific Corporation

Дата Авторизація:

2021-01-28

Характеристики продукта

Boston Scientific (DFU Template 3.25in x 4.5in Global), DFU, MB,
ACUITY Pro 9F, Global, 90981226-01B
2020-02
9F Guide Catheter
ACUITY
™ PRO
for use with
ACUITY™ PRO
Lead Delivery System
DIRECTIONS FOR USE.....................2
INSTRUCCIONES DE USO..............10
MODE D’EMPLOI ........................19
GEBRAUCHSANWEISUNG............28
ISTRUZIONI PER L’USO ..................37
GEBRUIKSAANWIJZING ...............46
BRUGSANVISNING .......................55
ΟΔΗΓΊΕΣ ΧΡΉΣΗΣ ....................64
INSTRUÇÕES DE UTILIZAÇÃO .......74
BRUKSANVISNING .......................83
HASZNÁLATI ÚTMUTATÓ ...........92
NÁVOD K POUŽITÍ ..................101
SPOSÓB UŻYCIA .....................110
BRUKSANVISNING .....................119
사용 지침 ..............................128
KULLANMA TALIMATLARI ........137
NÁVOD NA POUŽITIE .............146
ИНСТРУКЦИИ ПО
ПРИМЕНЕНИЮ ......................155
使用说明................................ 165
90981226-01
2
Boston Scientific (DFU Template 3.25in x 4.5in Global), DFU, MB,
ACUITY Pro 9F, Global, 90981226-01B
ONLY
CAUTION: Federal Law (USA) restricts this device to sale by or on the
order of a physician.
WARNING
Contents supplied STERILE using an ethylene oxide (EO) 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