特价供应ARROW箭牌泰利福主动脉内球囊反搏导管及附件各型号
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特价供应ARROW箭牌泰利福主动脉内球囊反搏导管及附件各型号
桂经理19117326863微xin同号
型号IAB-06830-U,IAB-06840-U,IAB-S730C,IAB-S840C,IAB-05840-U,IAB-R950-U,IAB-05830-U
从这项技术问世到现在，在心脏内科、外科所涉及的多种重症场景都发挥了重要作用。依据它设计的原理
目前临床中最常用于救治：
①急性心肌梗死合并心源性休克；
②急性心肌梗死后合并机械性并发症，如乳头肌功能不全、室间隔穿孔等；
③不稳定性心绞痛和顽固性心肌缺血等待手术治疗前；
④因心肌缺血或心脏功能衰竭导致的严重心律失常发作时；
⑤心脏手术后出现心脏泵衰竭；
⑥高危心脏手术术前/术中使用，减少手术风险；
⑦心脏移植手术过渡；
⑧右心衰竭患者的支持治疗等。
所以，对于心脏重症患者或心脏手术高危患者，IABP是个非常重要的拐棍，提高了重症患者走过悬崖的机会
主动脉内球囊反搏治疗使用时要注意什么？
尽管这项技术救治了非常多的重症心脏患者，但它也不是万能的，而且在治疗过程中也会带来一些风险，
比如增加血源性感染、下肢静脉血栓发生风险、下肢动脉缺血等风险。
因此，在使用前专科医生会进行充分考虑，选择合适的场景使用，也尽量缩短使用时长。
总之，目前主动脉内球囊反搏治疗仅局限于高风险、心功能严重受损和血流动力学不稳定的患者。
主动脉内球囊反搏治疗的历史悠久，19世纪80年代开始在临床上使用，
但它仍在当前国情和医疗环境下，在冠心病患者的治疗中占有重要的一席之地。
它作为一个能维持生命的有创机械治疗，需要更多的人们去了解这项技术的存在。
一、产品特点（Product Features）
中文
多规格适配：提供 30cc、40cc、50cc 三种球囊容积，适配不同身高 / 体表面积患者。
亲水涂层：球囊 / 导管表面亲水涂层，减少插入阻力与血管损伤风险Teleflex。
抗扭结设计：金属丝 / 线圈增强管身，提升推送性与抗折性Teleflex。
大腔设计：中央大腔（0.027"），减少导管摆动，保障压力监测与导丝通过Teleflex。
快速充放气：大口径接头，支持 30/40cc 最高 200bpm、50cc 最高 180bpm 氦气交换。
光纤传感（FiberOptix™）：双路高精度动脉压传感，支持 IntraBeat™时序控制Teleflex。
一次性灭菌：环氧乙烷灭菌，无菌独立包装，有效期 2 年。
配套齐全：含导管托盘、穿刺托盘、连接管、导丝、扩张器等完整套件。
English
Multi-size Adaptation: 30cc, 40cc, 50cc balloon volumes for patients of different heights/BSA.
Hydrophilic Coating: Reduces insertion resistance and vascular injury riskTeleflex.
Kink-resistant Design: Wire/coil reinforcement for improved pushabilityTeleflex.
Large Central Lumen: 0.027" ID minimizes catheter whip, supports pressure monitoringTeleflex.
High-rate Helium Exchange: Up to 200 bpm (30/40cc) / 180 bpm (50cc) via large-bore connector.
FiberOptix™ Sensing: Dual high-fidelity AP sensing for IntraBeat™ timingTeleflex.
Sterile & Single-use: EO-sterilized, 2-year shelf life.
Complete Kit: Catheter tray, insertion tray, tubing, guidewires, dilators included.
二、技术参数（Technical Parameters）
中文（核心型号）
表格
| 型号 | 球囊容积 | 导管规格 | 插入长度 | 球囊长度 | 中央腔内径 | 最大导丝 | 充气直径 | 适用鞘管 |
|---|---|---|---|---|---|---|---|---|
| IAB-06830-U | 30cc | 7.5Fr | 60.5cm | 230mm | 0.027" | 0.025" | 13.9mm | 7.5Fr |
| IAB-06840-U | 40cc | 7.5Fr | 66.0cm | 260mm | 0.027" | 0.025" | 15.0mm | 7.5Fr |
| IAB-05830-U | 30cc | 8.0Fr | 60.5cm | 230mm | 0.027" | 0.025" | 13.9mm | 8.0Fr |
| IAB-05840-U | 40cc | 8.0Fr | 66.0cm | 260mm | 0.027" | 0.025" | 15.0mm | 8.0Fr |
| IAB-R950-U | 50cc | 9.0Fr | 69.3cm | 260mm | 0.027" | 0.025" | 16.0mm | 9.0Fr |
球囊材料：Cardiothane II（聚氨酯 / 尼龙复合）
管身材料：聚酰亚胺 / 聚氨酯 + 不锈钢增强
充放气介质：氦气（快速、高溶解度）
灭菌方式：环氧乙烷（EO）灭菌
有效期：2 年
English (Key Models)
表格
| Model | Balloon Volume | French Size | Insertable Length | Balloon Length | Central Lumen ID | Max Guidewire | Inflated Diameter | Sheath Size |
|---|---|---|---|---|---|---|---|---|
| IAB-06830-U | 30cc | 7.5Fr | 60.5cm | 230mm | 0.027" | 0.025" | 13.9mm | 7.5Fr |
| IAB-06840-U | 40cc | 7.5Fr | 66.0cm | 260mm | 0.027" | 0.025" | 15.0mm | 7.5Fr |
| IAB-05830-U | 30cc | 8.0Fr | 60.5cm | 230mm | 0.027" | 0.025" | 13.9mm | 8.0Fr |
| IAB-05840-U | 40cc | 8.0Fr | 66.0cm | 260mm | 0.027" | 0.025" | 15.0mm | 8.0Fr |
| IAB-R950-U | 50cc | 9.0Fr | 69.3cm | 260mm | 0.027" | 0.025" | 16.0mm | 9.0Fr |
Balloon Material: Cardiothane II (Polyurethane/Nylon composite)
Catheter Material: Polyimide/Polyurethane + stainless steel reinforcement
Inflation Medium: Helium (fast, high solubility)
Sterilization: Ethylene Oxide (EO)
Shelf Life: 2 years
三、使用方法（Instructions for Use）
中文
术前准备
评估患者适应症 / 禁忌症，选择合适球囊规格（30/40/50cc）。
无菌操作，准备 IABP 主机、氦气、压力传感器、肝素盐水。
股动脉穿刺（Seldinger 技术），置入导丝与鞘管。
导管置入
沿导丝送入 IAB 导管，球囊顶端置于左锁骨下动脉开口下方 2cm、肾动脉开口上方。
X 线 / 透视确认位置（第二、三肋间水平）。
连接反搏泵与压力监测管路，排气、校准。
反搏启动
选择触发模式（ECG / 动脉压 / 起搏），设置 1:1/1:2 等反搏比。
舒张期充气、收缩期放气，监测动脉压波形与冠脉灌注改善。
术中监测
持续监测心率、血压、球囊位置、肢体血运、出血 / 血栓风险。
警惕球囊破裂、导管扭结、下肢缺血等并发症。
撤管与护理
逐步降低反搏比至 1:2/1:4，病情稳定后停机拔管。
局部压迫止血，监测穿刺点与下肢血运。
English
Preoperative Preparation
Evaluate indications/contraindications; select balloon size (30/40/50cc).
Sterile setup: IABP console, helium, pressure transducer, heparinized saline.
Femoral artery puncture (Seldinger technique), guidewire/sheath insertion.
Catheter Insertion
Advance IAB over guidewire; position tip 2cm below left subclavian artery, above renal arteries.
Confirm placement via X-ray/fluoroscopy (2nd–3rd intercostal space).
Connect to pump/pressure lines; purge air, calibrate.
Initiate Counterpulsation
Select trigger (ECG/AP/pacing), set assist ratio (1:1/1:2).
Inflate in diastole, deflate in systole; monitor waveｆorm and coronary perfusion.
Intraoperative Monitoring
Continuously monitor HR, BP, balloon position, limb perfusion, bleeding/thrombosis risk.
Watch for balloon rupture, kinking, lower limb ischemia.
Weaning & Removal
Gradually reduce assist ratio to 1:2/1:4; wean and remove when stable.
Apply pressure hemostasis; monitor puncture site and limb perfusion.
四、适应症（Indications）
中文
急性心肌梗死合并心源性休克
难治性不稳定型心绞痛
高危 PCI / 冠脉介入循环支持
心脏 / 非心脏手术围术期心功能支持
低心排综合征、心肌功能障碍
心肌梗死机械并发症（室间隔穿孔、乳头肌断裂）
脱离体外循环困难、术后低心排
English
Acute MI with cardiogenic shock
Refractory unstable angina
High-risk PCI/coronary intervention support
Perioperative cardiac support (cardiac/non-cardiac surgery)
Low cardiac output syndrome, myocardial dysfunction
Mechanical complications of MI (VSD, papillary muscle rupture)
Difficulty weaning from CPB, post-op low cardiac output
五、禁忌症（Contraindications）
中文
主动脉夹层、主动脉瘤、主动脉窦瘤破裂
中重度主动脉瓣关闭不全
严重主动脉 - 髂动脉闭塞 / 狭窄病变
未控制的严重凝血功能障碍
脑出血急性期、严重贫血
终末期疾病、预期生存极短
English
Aortic dissection, aneurysm, sinus of Valsalva rupture
Moderate–severe aortic regurgitation
Severe aorto-iliac occlusive disease
Uncontrolled severe coagulopathy
Acute intracerebral hemorrhage, severe anemia
Terminal illness with very short life expectancy
六、注意事项（Precautions）
中文
无菌操作：全程严格无菌，避免感染。
球囊定位：X 线确认位置，避免移位 / 阻塞冠脉 / 肾动脉。
充放气控制：同步，避免充气过早 / 过晚导致心肌缺血或后负荷增加。
抗凝管理：规范肝素化，监测 ACT/APTT，预防血栓 / 出血。
并发症监测：下肢缺血、球囊破裂、导管扭结、感染、出血等。
撤管规范：逐步减停反搏，避免突然停机导致血流动力学波动。
一次性使用：严禁重复灭菌 / 使用，防止交叉感染。
English
Sterile Technique: Maintain strict asepsis to prevent infection.
Balloon Position: Confirm via X-ray; avoid displacement/occlusion of coronals/renal arteries.
Timing Control: Precise synchronization; avoid early/late inflation causing ischemia/afterload rise.
Anticoagulation: Standard heparinization; monitor ACT/APTT to prevent thrombosis/bleeding.
Complication Monitoring: Limb ischemia, balloon rupture, kinking, infection, bleeding.
Weaning Protocol: Gradual reduction; avoid abrupt weaning to prevent hemodynamic instability.
Single-use Only: Do not re-sterilize/reuse; risk of cross-infection.
七、存储条件（Storage Conditions）
中文
温度：15–30℃（59–86°F）
湿度：相对湿度 30%–70%
避免：阳光直射、高温、潮湿、腐蚀性气体
包装：保持原包装完整、干燥、无菌
有效期：包装标注日期内使用（通常 2 年）
English
Temperature: 15–30°C (59–86°F)
Humidity: 30%–70% RH
Avoid: Direct sunlight, extreme heat, moisture, corrosive gases
Packaging: Keep original package intact, dry, sterile
Shelf Life: Use before expiration date (typically 2 years)
八、说明书核心信息（IFU Key Points）
中文
产品概述：用于主动脉内球囊反搏（IABP），舒张期充气增加冠脉灌注，收缩期放气降低左室后负荷。
规格选择：按身高 / BSA 选 30/40/50cc，临床医师最终决策。
操作资质：接受专业培训的医师 / 医护人员使用。
安全警示：
一次性使用，严禁重复灭菌。
球囊破裂立即停机，抗凝并拔管。
避免暴力操作，防止血管撕裂 / 导管损坏。
并发症处理：下肢缺血、出血、感染、血栓等按临床指南处理。
责任声明：本资料为摘要，完整信息以原厂说明书为准。
English
Product Overview: For IABP therapy; inflate in diastole to increase coronary perfusion, deflate in systole to reduce LV afterload.
Sizing: Select 30/40/50cc by height/BSA; final decision by clinician.
User Qualification: For use only by trained physicians/medical staff.
Safety Warnings:
Single-use; do not re-sterilize.
Stop pump immediately if balloon ruptures; anticoagulate and remove catheter.
Avoid forceful manipulation to prevent vascular injury/catheter damage.
Complication Management: Treat limb ischemia, bleeding, infection, thrombosis per clinical guidelines.
Disclaimer: Summary only; full details in official IFU.
Shanghai
Kangshida Medical Devices Co., Ltd. is a professional company engaged in
the sales of medical devices,
focusing on the agency and distribution
of renowned medical equipment brands from both domestic and
international markets. Its core product range covers full-scenario
medical devices for physical examination,
diagnosis, emergency
treatment, laboratory testing, ultrasound, medical analysis, life
sciences, disinfection
and sterilization, rehabilitation therapy,
operating rooms, emergency rooms, consulting rooms and other fields.
Relying on its strong product sales capacity, excellent commercial
reputation and integrity-based operation
philosophy, the company has won
unanimous recognition and trust from medical institutions and partners.
The
steady and rapid development of the company is attributed to its
carefully selected high-quality product
portfolio. It always takes
customer needs as the core orientation and is committed to creating
long-term value
and practical benefits for customers. As an authorized
and exclusive agent for many well-known domestic
and international
manufacturers, the company has established a complete supply system of
medical devices
with reliable quality, fully meeting the needs of
clinical diagnosis and treatment.
The company always takes improving
customer satisfaction as its core goal. To strictly adhere to product
standards and exceed the expectations of customers and manufacturers, it
regularly provides training on
professional ethics and professional
business skills, forging a highly competent, efficient and executive
team covering business, technology and management. The team implements a
7×24-hour all-weather response
mechanism to provide professional and
high-quality after-sales service and technical support, efficiently
solving various equipment operation and maintenance problems. At the
same time, the company offers exclusive
services including same-day
delivery and free distribution, ｆorming a closed loop covering supply,
distribution
and after-sales service to fully ensure the stable supply
and worry-free use of medical equipment for medical
institutions.
Upholding
integrity as the foundation of its business, the company selects
high-quality medical devices and
provides professional services for
customers, helping to upgrade the quality of medical services and
contributing to the high-quality development of China's medical
industry.
Intellectual Property Infringement Complaint: Kangshida
Medical does not manufacture medical products;
all products are sourced
from original manufacturers. We will promptly address any intellectual
property
infringement issues.
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