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扬州富达医疗器械有限公司

境内医疗器械(注册) — “苏械注准20222020583”基本信息
注册证编号苏械注准20222020583 [查看相关产品信息]
注册人名称扬州富达医疗器械有限公司[查看公司信息]
注册人住所扬州头桥镇红桥工业园区
生产地址扬州头桥镇红桥工业园区
产品名称一次性使用内窥镜给药管
管理类别第二类
型号规格FD/PSG-W1812,FD/PSG-W1816,FD/PSG-W1818,FD/PSG-W1820,FD/PSG-W1823,FD/PSG-W2012,FD/PSG-W2016,FD/PSG-W2018,FD/PSG-W2020,FD/PSG-W2023,FD/PSG-W2412,FD/PSG-W2416,FD/PSG-W2418,FD/PSG-W2420,FD/PSG-W2423FD/PSG-L1812,FD/PSG-L1816,FD/PSG-L1818,FD/PSG-L1820,FD/PSG-L1823,FD/PSG-L2012,FD/PSG-L2016,FD/PSG-L2018,FD/PSG-L2020,FD/PSG-L2023,FD/PSG-L2412,FD/PSG-L2416,FD/PSG-L2418,FD/PSG-L2420,FD/PSG-L2423FD/PSG-Z1812-2104,FD/PSG-Z1812-2106,FD/PSG-Z1812-2304,FD/PSG-Z1812-2306,FD/PSG-Z1812-2504,FD/PSG-Z1812-2506,FD/PSG-Z1816-2104,FD/PSG-Z1816-2106,FD/PSG-Z1816-2304,FD/PSG-Z1816-2306,FD/PSG-Z1816-2504,FD/PSG-Z1816-2506,FD/PSG-Z1820-2104,FD/PSG-Z1820-2106,FD/PSG-Z1820-2304,FD/PSG-Z1820-2306,FD/PSG-Z1820-2504,FD/PSG-Z1820-2506,FD/PSG-Z1823-2104,FD/PSG-Z1823-2106,FD/PSG-Z1823-2304,FD/PSG-Z1823-2306,FD/PSG-Z1823-2504,FD/PSG-Z1823-2506FD/PSG-Z2416-2104,FD/PSG-Z2416-2106,FD/PSG-Z2416-2304,FD/PSG-Z2416-2306,FD/PSG-Z2416-2504,FD/PSG-Z2416-2506,FD/PSG-Z2418-2104,FD/PSG-Z2418-2106,FD/PSG-Z2418-2304,FD/PSG-Z2418-2306,FD/PSG-Z2418-2504,FD/PSG-Z2418-2506,FD/PSG-Z2420-2104,FD/PSG-Z2420-2106,FD/PSG-Z2420-2304,FD/PSG-Z2420-2306,FD/PSG-Z2420-2504,FD/PSG-Z2420-2506,FD/PSG-Z2423-2104,FD/PSG-Z2423-2106,FD/PSG-Z2423-2304,FD/PSG-Z2423-2306,FD/PSG-Z2423-2504,FD/PSG-Z2423-2506
结构及组成/主要组成成分一次性使用内窥镜给药管是由头部、导管和手柄组件组成。根据灌注装置型式不同分为雾状、直线状和局部雾状;根据外管直径、工作长度不同分为若干规格。该产品以无菌状态提供,经环氧乙烷灭菌。一次性使用。
适用范围/预期用途与内窥镜配合使用,用于对人体腔道进行液体输送、灌洗、喷射等操作。(不用于人体注射)
审批部门江苏省药品监督管理局
批准日期2022/1/20
生效日期2022/1/20
有效期至2027/1/19
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