厂商直销箭牌血液透析用中心静脉导管套件CS-26122-F
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厂商直销箭牌血液透析用中心静脉导管套件CS-26122-F
桂经理19117326863微xin同号
桂经理19117326863微xin同号
管理类别
第三类
型号规格
CS-22122-F,CS-22142-CF,CS-22142-F,CS-25142-CF,CS-25142-F,CS-26122-F,CU-22122-F,CS-25122-F,CU-23122-F,CU-25122-F
结构及组成/主要组成成分
血液透析用中心静脉导管套件包括中心静脉导管、导管夹、导丝、手术刀片、套管针、穿刺针、导引套管、组织扩张器、导引注射器、测压探针、辅巾、防尘帽、缝合翼。导管表面涂有磺胺嘧啶银和洗必泰的涂层。产品经环氧乙烷灭菌。
适用范围/预期用途
该产品可允许从静脉进入中心血液循环,以此实现快速输液、临时或急性血液透析、血液成分分离和血液净化。这种导管可插入颈静脉、锁骨下静脉或股静脉内。
1、工作原理 Working Principle
中文: 套件采用 Seldinger 经皮穿刺技术,将双腔不透射线聚氨酯导管置入中心静脉;双腔相互独立,一腔引出血液(动脉腔)、一腔回输净化后血液(静脉腔),建立中心血管通路,实现体外血液循环;导管外表面搭载 Arrowg+ard Blue 抗菌涂层,降低导管相关血流感染风险。
English: Adopt Seldinger percutaneous puncture technique to place dual‑lumen radiopaque polyurethane catheter into central vein. Two independent lumens: one for blood withdrawal (arterial lumen), another for returning purified blood (venous lumen), establishing central vascular access for extracorporeal blood circulation. The outer surface is coated with Arrowg+ard Blue antimicrobial coating to reduce risk of catheter‑associated bloodstream infection (CLABSI).
2、功能 Function
中文
建立短期中心静脉血管通路,满足急性 / 临时血液透析、血液成分分离、血液滤过;
支持大容量快速静脉输液;
可用于中心静脉压力监测、采血;
抗菌涂层抑制导管表面致病菌定植;
整套套件包含全套穿刺置入器械,实现一站式置管操作。
English
Establish short‑term central venous access for acute/temporary hemodialysis, apheresis and hemofiltration.
Deliver high‑volume rapid intravenous infusion.
Support central venous pressure monitoring and blood sampling.
Antimicrobial coating inhibits pathogenic bacterial colonization on catheter surface.
Complete kit with full set of insertion instruments for one‑stop catheter placement.
3、产品特点 Product Features
中文
Arrowg+ard Blue 抗菌表面涂层(醋酸洗必泰 + 磺胺嘧啶银),广谱抗菌,降低 CLABSI 发生率Teleflex I...;
Blue FlexTip 蓝色柔性软头,减少血管内膜损伤;
双腔大流量设计,适配透析高血流需求;
导管为不透射线聚氨酯材质,X 光下显影,带有厘米深度刻度;
延伸管自带导管夹,可阻断管路;
全套 Seldinger 器械:穿刺针、弹簧导丝、组织扩张器、手术刀、辅巾、防尘帽、缝合翼等,开箱即用;
环氧乙烷灭菌,一次性无菌使用;
MR 条件安全(MR Conditional)。
English
Arrowg+ard Blue antimicrobial surface coating (chlorhexidine acetate + silver sulfadiazine), broad‑spectrum antibacterial to lower CLABSI incidenceTeleflex I....
Blue FlexTip soft flexible tip to minimize intimal vessel injury.
Dual‑lumen high‑flow design for hemodialysis high blood flow requirement.
Radiopaque polyurethane catheter with centimeter depth markings for X‑ray visualization.
Extension lines equipped with clamps for line occlusion.
Complete Seldinger instrument set: introducer needle, spring‑tip guidewire, tissue dilator, scalpel, drape, dust caps, suture wings, ready‑to‑use.
EO sterilized, single‑use sterile device.
MR Conditional.
4、技术参数 Technical Specifications
表格
| 中文参数 | English Specifications |
|---|---|
| 型号 Model | CS‑26122‑F |
| 导管外径 Outer Diameter | 12 Fr(4.06 mm) |
| 导管总长度 Catheter Length | 25 cm |
| 导管材质 Catheter Material | 不透射线聚氨酯 Radiopaque Polyurethane |
| 涂层 Coating | Arrowg+ard Blue(醋酸洗必泰、磺胺嘧啶银) Arrowg+ard Blue (chlorhexidine acetate, silver sulfadiazine) |
| 导丝 Guidewire | 0.035"(0.89 mm),长度 68 cm,一端直软头、一端 J 头 0.035"(0.89 mm), 68 cm length, straight soft tip / J‑tip dual ends |
| 组织扩张器 Tissue Dilator | 12 Fr,14 cm |
| 预充体积 Priming Volume | 远端腔约 1.8 mL;近端腔约 1.7 mL Distal lumen ≈1.8 mL; Proximal lumen ≈1.7 mL |
| 最大血流速率 Max Blood Flow | 约 300 mL/min(静脉压 100‑200 mmHg 下) Approx. 300 mL/min @ 100‑200 mmHg venous pressure |
| 灭菌方式 Sterilization | 环氧乙烷 Ethylene Oxide (EO) |
| 适用留置时长 Intended Dwell Time | 短期<30 天 Short‑term<30 days |
| 套件包含 Components | 双腔导管、导管夹、弹簧导丝、导引针、导引注射器、组织扩张器、#11 手术刀、测压探针、手术辅巾、防尘帽、缝合翼 Two‑lumen catheter, clamps, spring guidewire, introducer needle, introducer syringe, tissue dilator, #11 scalpel, pressure transduction probe, drape, dust caps, suture wingsTeleflex I... |

5、使用方法 Instructions for Use(核心步骤摘要)
中文
核对包装完好、灭菌有效期,确认型号无误;本产品仅供经皮 Seldinger 技术置管;
选择置管静脉(颈内静脉 / 锁骨下静脉 / 股静脉),执行标准无菌最大屏障防护;
穿刺针穿刺目标静脉,回抽见血确认在血管内;置入弹簧导丝,撤出穿刺针;
手术刀做皮肤小切口,组织扩张器沿导丝扩张皮下及血管入口,撤出扩张器;
将双腔导管沿导丝送入中心静脉,调整至合适深度;撤出导丝;
两腔分别回抽见血,生理盐水冲洗管腔;缝合翼固定导管于皮肤;安装防尘帽;
影像学确认导管尖端位置到位后,方可用于透析 / 输液;
使用后按临床规范冲管封管;留置不超过 30 天;到期需拔除;
一次性使用,严禁重复灭菌复用。
English
Verify package integrity, sterilization expiry and correct model. For percutaneous Seldinger technique only.
Select access vein (internal jugular / subclavian / femoral vein), apply full sterile maximal barrier precaution.
Puncture target vein with introducer needle; confirm intravascular position by blood aspiration. Insert spring guidewire, remove needle.
Make small skin incision with scalpel; dilate subcutaneous tissue and vessel entry with tissue dilator over guidewire; remove dilator.
Advance dual‑lumen catheter over guidewire into central vein to proper depth; withdraw guidewire.
Aspirate blood from both lumens; flush lumens with normal saline; secure catheter to skin with suture wings; fit dust caps.
Confirm catheter tip position by imaging prior to hemodialysis / infusion use.
Perform standardized lumen flushing and locking after use. Dwell time shall not exceed 30 days; remove catheter at end of indication.
Single‑use only. Do not re‑sterilize or reuse.

6、适应症 Indications for Use
中文本套件用于建立短期(<30 天)中心静脉血管通路:
急性、临时血液透析;
血液成分分离、血液滤过等血液净化治疗;
大容量快速静脉输液给药;
中心静脉采血、中心静脉压监测;
可置入颈内静脉、锁骨下静脉或股静脉。
EnglishThis kit establishes short‑term (<30 days) central venous vascular access:
Acute or temporary hemodialysis.
Apheresis, hemofiltration and other blood purification therapies.
High‑volume rapid intravenous fluid and drug administration.
Central venous blood sampling and central venous pressure monitoring.
May be placed in internal jugular vein, subclavian vein or femoral vein.
7、禁忌症 Contraindications
中文
已知对醋酸洗必泰、磺胺嘧啶银、磺胺类药物、导管材料聚氨酯过敏患者;
目标置管静脉血栓形成、血管闭塞;
穿刺局部皮肤感染、烧伤、破损;
不用于超过 30 天长期透析通路;
严重凝血功能障碍,穿刺出血风险不可控;
血管解剖畸形无法安全穿刺置管。
English
Known hypersensitivity to chlorhexidine acetate, silver sulfadiazine, sulfa‑drugs or catheter polyurethane material.
Thrombosis or occlusion of target access vein.
Local skin infection, burn or lesion at puncture site.
Not intended for long‑term hemodialysis access over 30 days.
Severe coagulopathy with uncontrollable bleeding risk at puncture site.
Vascular anatomical malformation preventing safe percutaneous placement.

8、注意事项 Warnings & Precautions
中文
受过中心静脉置管专业培训医师操作;严格无菌操作,落实最大无菌屏障;
包装破损、潮湿、过期禁止使用;一次性,严禁复用、重复灭菌;
置管全程警惕并发症:气胸、血胸、血管损伤、出血、空气栓塞、心律失常、导管异位;推荐置管后影像学确认导管尖端位置;
抗菌涂层仅降低感染风险,不能完全消除感染,仍需执行导管维护集束化方案;
留置时间不超过 30 天,超时必须拔除;
操作时保护导丝,防止导丝脱落、误入血管;
管路夹必须保持完好;透析、输液前确认管路通畅;
导管不可用于高压造影注射;
出现发热、穿刺处红肿渗液、血流不足、血栓迹象及时评估处理;
MR 条件安全,遵循原厂 MR 相关说明;
废弃按照医疗感染性废物处置。
English
Only operated by physicians with formal central venous catheter insertion training. Strict aseptic technique with maximal sterile barrier precautions.
Do not use if package is damaged, damp or expired. Single‑use only; re‑use and re‑sterilization are prohibited.
Be alert for complications: pneumothorax, hemothorax, vessel injury, hemorrhage, air embolism, arrhythmia, catheter malposition. Imaging confirmation of catheter tip after placement is recommended.
Antimicrobial coating reduces but cannot eliminate infection risk; catheter bundle maintenance protocol shall still be followed.
Dwell time shall not exceed 30 days; catheter must be removed beyond this period.
Secure guidewire during whole procedure to prevent guidewire loss into vessel.
Keep extension clamps functional; confirm patency prior to hemodialysis or infusion.
Catheter shall NOT be used for high‑pressure contrast media injection.
Prompt clinical evaluation for fever, local erythema/drainage, insufficient blood flow or suspected thrombosis.
MR Conditional; follow manufacturer MR guidance.
Dispose as bio‑hazard medical waste.
9、存储条件 Storage Conditions
中文
存储环境温度低于 25 ℃;避免超过 40 ℃高温环境;
存放于干燥通风处,避光,远离腐蚀性气体;
不可重压、撞击包装;
在有效期内使用。
English
Store below 25 ℃, avoid excessive heat above 40 ℃.
Store in dry, ventilated place, protected from light and corrosive gas.
Prevent heavy compression or impact to package.
Use within shelf‑life expiry date.

10、产品基础注册信息 Basic Registration Info
产品名称:血液透析用中心静脉导管套件 / Two‑Lumen Hemodialysis Catheterization Kit
型号:CS‑26122‑F
注册人:Arrow International LLC(箭牌国际公司,Teleflex 旗下)
国内代理人:泰利福医疗器械商贸(上海)有限公司
注册证编号:国械注进 20163100668
免责提示:以上产品详情仅供参考,临床操作请以原厂纸质说明书为准。上海康世达医疗器械有限公司不生产医疗产品,所有产品均来自产品的生产厂家,代理商,经销商,如有侵权请联系我们,会尽快处理!The above product details are for reference only. All clinical operations shall be carried out in strict accordance with the original paper instructions for use issued by the manufacturer.
Shanghai Kangshida Medical Devices Co., Ltd. does not manufacture medical devices. All products are sourced from respective manufacturers, authorized agents and distributors.
Please contact us promptly in case of any infringement, and we will resolve the matter as soon as possible.
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