成都普什医疗科技有限公司
境内医疗器械（注册） — “川械注准20212220138”基本信息
| 注册证编号 | 川械注准20212220138 [查看相关产品信息] |
| 注册人名称 | 成都普什医疗科技有限公司[查看公司信息] |
| 注册人住所 | 成都高新区（西区）科新路6号1栋、2栋 |
| 生产地址 | 成都高新西区科新路6号1栋A座3楼、2栋、4栋 |
| 产品名称 | 一次性使用微量采血管 |
| 管理类别 | 第二类 |
| 型号规格 | PS/WLCXG NH 8×45mm/0.25ml PP、PS/WLCXG NH 8×45mm/0.5ml PP PS/WLCXG NH 11×45mm/0.25ml PP、PS/WLCXG NH 11×45mm/0.5ml PP PS/WLCXG LH 8×45mm/0.25ml PP、PS/WLCXG LH 8×45mm/0.5ml PP PS/WLCXG LH 11×45mm/0.5ml PP、PS/WLCXG LH 11×45mm/0.25ml PP PS/WLCXG 无添加剂 8×45mm/0.25ml PP、PS/WLCXG 无添加剂 8×45mm/0.5ml PP PS/WLCXG 无添加剂 11×45mm/0.25ml PP、PS/WLCXG 无添加剂 11×45mm/0.5ml PP PS/WLCXG 促凝剂 8×45mm/0.25ml PP、PS/WLCXG 促凝剂 8×45mm/0.5ml PP PS/WLCXG 促凝剂 11×45mm/0.25ml PP、PS/WLCXG 促凝剂 11×45mm/0.5ml PP PS/WLCXG 分离胶 8×45mm/0.25ml PP、PS/WLCXG 分离胶 8×45mm/0.5ml PP PS/WLCXG 分离胶 11×45mm/0.25ml PP、PS/WLCXG 分离胶 11×45mm/0.5ml PP PS/WLCXG K2E 8×45mm/0.25ml PP、PS/WLCXG K2E 8×45mm/0.5ml PP PS/WLCXG K2E 11×45mm/0.25ml PP、PPPS/WLCXG K2E 11×45mm/0.5ml PP PS/WLCXG K3E 8×45mm/0.25ml PP、PS/WLCXG K3E 8×45mm/0.5ml PP PS/WLCXG K3E 11×45mm/0.25ml PP、PS/WLCXG K3E 11×45mm/0.5ml PP PS/WLCXG N2E 8×45mm/0.25ml PP、PS/WLCXG N2E 8×45mm/0.5ml PP PS/WLCXG N2E 11×45mm/0.25ml PP、PS/WLCXG N2E 11×45mm/0.5ml PP PS/WLCXG FX 8×45mm/0.25ml PP、PS/WLCXG FX 8×45mm/0.5ml PP PS/WLCXG FX 11×45mm/0.25ml PP、PS/WLCXG FX 11×45mm/0.5ml PP PS/WLCXG FE 8×45mm/0.25ml PP、PS/WLCXG FE 8×45mm/0.5ml PP PS/WLCXG FE 11×45mm/0.25ml PP、PS/WLCXG FE 11×45mm/0.5ml PP PS/WLCXG FH 8×45mm/0.25ml PP、PS/WLCXG FH 8×45mm/0.5ml PP PS/WLCXG FH 11×45mm/0.25ml PP、PS/WLCXG FH 11×45mm/0.5ml PP |
| 结构及组成/主要组成成分 | 一次性使用微量采血管由试管、塑料防溅帽以及有或无添加剂组成。试管为聚丙烯（PP）材质，塑料防溅帽为聚乙烯（PE）材质。产品为非无菌。 |
| 适用范围/预期用途 | 用于人体末梢血样的采集、运输和储存。 |
| 审批部门 | 四川省药品监督管理局 |
| 批准日期 | 2021/6/16 |
| 生效日期 | 2021/6/16 |
| 有效期至 | 2026/6/15 |
