Specification

विशेषताएँ
High ultrafiltration rate, high clearance for plasma water, low priming volume, biocompatible and pyrogen-free

माप सीमा
Ultrafiltration rate up to 0.2 L/min

स्टोरेज निर्देश
Store in cool, dry place away from sunlight

इंस्ट्रूमेंट्स टाइप
Extracorporeal blood purification device

शेल्फ लाइफ
3-5 years (unopened, sterile)

सटीकता
High (membrane separation)

फंक्शन
Removes excess plasma water and waste products from blood

उपयोग का प्रकार
Hospital/Clinical

मटेरियल

शर्त

टेक्नोलॉजी
Hollow fiber membrane filtration

पोर्टेबल
Yes

वॉल माउंटेड

रियल-टाइम ऑपरेशन

शोर का स्तर
Silent operation

ऑपरेटिंग टाइप

उपयोग करें
Hemoconcentration during Cardiopulmonary Bypass

पावर सोर्स

आयाम (एल* डब्ल्यू* एच)
Approx. 300 mm length, 42 mm diameter

वज़न
Approx. 220 g

रंग
Transparent/White

About

ADULT : EFFECTIVE SURFACE AREA 0.9 m² AND FOR THAT MINIMUM PRIMING VOLUME 44 ml , MTP 600 mmHg

PEDIATRIC : EFFECTIVE SURFACE AREA 0.6 m² AND FOR THATMINIMUM PRIMING VOLUME 32 ml , MTP 600 mmHg

NEONATAL: EFFECTIVE SURFACE AREA 0.2 m² AND FOR THATMINIMUM PRIMING VOLUME 18 ml , MTP 600 mmHg

USER

For reference please note some hospitals as like UN Mehta Institute of Cardiology and ResearchCentre (Ahmedabad), Geetanjali Medical College & Hospital (Udaipur),NARAYAN HOSPITAL ( MUMBAI ) and many more counting ...

Advanced Hemoconcentration Technology

Utilizing hollow fiber membrane filtration, the Hemoconcentrator 0.2 delivers superior ultrafiltration and plasma water clearance. Its high-end PES membrane ensures efficient separation of plasma while retaining endotoxins, offering reliable, pyrogen-free purification during extracorporeal procedures. The device is suitable for adults and children, ensuring versatile clinical application.

Safety and Compliance

Manufactured from polycarbonate/polypropylene materials and sterilized with ethylene oxide (ETO), this device is latex-free, minimizing allergic reactions. It adheres to stringent CE and ISO standards, guaranteeing high accuracy and biocompatibility for patient safety. Its long shelf life and stable operation make it ideal for hospital and clinical use.

User-Friendly and Portable Design

The Hemoconcentrator's transparent, lightweight construction allows for effortless portability and integration in busy clinical environments. With standard Luer lock connectors, silent operation, and no external power requirements, clinicians can operate it manually or with an extracorporeal circuit for real-time blood water removal, enhancing workflow efficiency.

FAQ's of Hemoconcentrators 0.2:

Q: How is the Hemoconcentrator 0.2 used during cardiopulmonary bypass procedures?

A: The Hemoconcentrator 0.2 is connected to the extracorporeal blood circuit via standard Luer lock or tubing connections. It operates using the circuit's pressure to separate and remove excess plasma water and waste products, aiding in the management of fluid balance during cardiopulmonary bypass.

Q: What types of patients can benefit from this hemoconcentrator?

A: This device is designed for both adult and pediatric patients, as guided by clinical protocols. Its adjustable blood flow rate and high biocompatibility make it suitable for a wide range of clinical scenarios requiring extracorporeal blood purification.

Q: When should the hemoconcentrator be replaced or disposed of?

A: The Hemoconcentrator 0.2 is intended for single use only. It must be disposed of after each procedure to prevent contamination, in accordance with hospital waste management practices.

Q: Where should the Hemoconcentrator 0.2 be stored before use?

A: Store the device in a cool, dry place away from sunlight. Unopened and sterile units have a shelf life of three to five years under recommended storage conditions.

Q: What is the process for setting up the Hemoconcentrator 0.2 in a clinical environment?

A: Setup involves connecting the device's Luer lock or tubing connectors to the blood circuit, priming with approximately 45 mL, and ensuring proper temperature and operating conditions (15C-37C) before initiating ultrafiltration.

Q: What are the main benefits of using this hemoconcentrator?

A: Benefits include highly effective plasma water removal, reliable endotoxin retention, low priming volume, silent operation, high accuracy, and compatibility with standard hospital protocols-improving patient outcomes during extracorporeal procedures.

Q: Does the Hemoconcentrator 0.2 require an external power source for operation?

A: No external power source is needed; the device uses the blood circuit's pressure for real-time ultrafiltration, supporting seamless integration with manual or assisted extracorporeal systems.

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