![Stryker HH1001 Main Arm Скачать руководство пользователя страница 7](http://html.mh-extra.com/html/stryker/hh1001-main-arm/hh1001-main-arm_instructions-for-use-manual_1385926007.webp)
©2020 IFU-0100 / rev3
7
7. To maintain intended clamping capacity of the table rail
clamp, do not tighten the table rail clamping knob when
the main arm column is not fully installed.
8.
The Rail Clamps are not insulated. If grounding of patient
is NOT ACCEPTABLE, DO NOT use the system.
9.
DO NOT FORCE BLACK KNOB OF THE MAIN ARM
PAST STOP WHEN OPENING/LOOSENING.
6. Possible Adverse Effects
Delayed surgical procedure.
7. Storage
Components should be stored in a clean and dry area.
Inspect
each component prior to use for functionality and damage.
When necessary, dispose of products in accordance with
national regulations and approved hospital practices for
surgical component disposal.
8. Product Description and Use
8.1 Main Arm (HH1001)
Provides three-point positioning of the
imaging head into the surgical field. The
articulating segments of the Main Arm are
connected to a rigid column.
To position and lock in place:
1. Hold the distal end with one hand
and loosen the central knob by
turning it counterclockwise.
2. Position the imaging head as needed
and turn the knob clockwise to lock in
place. Check to see that the Main
Arm is secure enough to hold its
position.
8.2 Table Clamp (HH1002)
Provides an attachment point to the operating table side rail.
Accepts and holds the column of the main arm in position
and allows for full range of rotation.
Содержание HH1001 Main Arm
Страница 202: ... 2020 IFU 0100 rev3 202 1 定義 記号説明 参照番号 バッチコード 製品数量 欧州医療機器規則に準拠 製造年月日 製造業者 欧州共同体域内の販売責任者 未滅菌で供給される製品 製品が医療機器であることを示す ...
Страница 212: ... 2020 IFU 0100 rev3 212 ...
Страница 225: ... 2020 IFU 0100 rev3 225 800 624 4422 수신자 부담 전화 미국 전용 또는 이메일 EndoCustomerSupport stryker com ...
Страница 228: ... 2020 IFU 0100 rev3 228 1 定义 符号说明 产品编号 批号 产品数量 符合欧盟医疗器械法规 制造日期 制造商 欧盟授权代表 非无菌产品 表示产品为医疗器械 ...
Страница 238: ... 2020 IFU 0100 rev3 238 1 定義 符號說明 參考號碼 批號 產品數量 符合歐洲醫療器材法規 製造日期 製造商 歐盟授權代表 產品出貨時並未滅菌 所示產品為一醫療器材 ...