Question 1

What is a cardiac oxygenator?

Accepted Answer

A cardiac oxygenator is a single-use device in a cardiopulmonary bypass circuit that adds oxygen to blood and removes carbon dioxide while the heart and lungs are supported during surgery.

Question 2

How is an oxygenator different from a ventilator?

Accepted Answer

A ventilator moves gas into and out of the lungs. An oxygenator performs gas exchange directly with blood outside the body as part of a bypass or extracorporeal circuit.

Question 3

Which oxygenator is suitable for an adult, paediatric or neonatal patient?

Accepted Answer

Selection depends on rated blood-flow range, prime volume, gas-transfer performance, heat exchanger, coating, circuit compatibility and the manufacturerâ€™s instructions for use. A perfusion team must make the clinical selection.

Question 4

Are oxygenators reusable?

Accepted Answer

Cardiac oxygenators are generally sterile, single-use medical devices. Follow the label and instructions for use; reprocessing a single-use device can create serious safety and regulatory risks.

Question 5

What should a hospital check before buying oxygenators?

Accepted Answer

Confirm model, intended use, flow range, expiry, sterile packaging, storage conditions, lot traceability, regulatory documents, manufacturer authorization where applicable and compatibility with the planned circuit.

Question 6

What is a guide wire?

Accepted Answer

A guide wire is a thin, flexible device used to establish a path through a vessel or duct so that catheters, balloons, stents or other devices can be advanced.

Question 7

Is â€œguidewireâ€ the same as â€œguide wireâ€?

Accepted Answer

Yes. Both spellings are commonly used. The applicable product label and manufacturer documentation should be used for a specific device.

Question 8

What is a Runthrough guide wire?

Accepted Answer

Runthrough is a branded family of coronary guide wires used as workhorse wires in PCI. Buyers should verify the exact manufacturer, model, tip configuration, length and authorized supply status.

Question 9

What does 0.014 inch mean for a guide wire?

Accepted Answer

It is the nominal outer diameter commonly used for coronary intervention guide wires. Peripheral and other procedures may use different diameters.

Question 10

What is the difference between hydrophilic and hydrophobic guide-wire coatings?

Accepted Answer

Hydrophilic coatings become highly lubricious when wet, while hydrophobic or PTFE-style coatings provide different tactile and friction characteristics. Choice depends on anatomy, lesion and procedure.

Question 11

What is a workhorse coronary guide wire?

Accepted Answer

A workhorse wire is designed for routine PCI and balances steerability, torque response, support and an atraumatic distal tip. It is not suitable for every lesion.

Question 12

What is a CTO guide wire?

Accepted Answer

A CTO wire is designed for chronic total occlusion crossing and may have specialized tip loads, penetration characteristics or coatings. It should be used only by trained clinicians.

Question 13

What documentation should accompany guide wires?

Accepted Answer

Typical procurement documents include product label details, instructions for use, lot and expiry information, sterilization status, applicable regulatory registration and manufacturer or distributor documentation.

Question 14

What is a hemofilter?

Accepted Answer

A hemofilter is a blood purification filter used in renal replacement or fluid-management therapies. Its membrane allows controlled movement of water and selected solutes.

Question 15

Is a hemofilter the same as a hemodialyzer?

Accepted Answer

They are related blood purification devices but may be designed for different therapies, flow conditions and clearance mechanisms. Use the exact device indicated by the therapy protocol and manufacturer.

Question 16

How is a dialysis filter selected?

Accepted Answer

Selection considers therapy type, membrane, surface area, ultrafiltration coefficient, clearance data, blood volume, connector compatibility and patient-specific clinical requirements.

Question 17

Do you supply interventional cardiology products?

Accepted Answer

Availability may include guide wires, catheters, introducer accessories and related consumables. Contact the team with the required brand, model, size, quantity and destination for current confirmation.

Question 18

Which cardiac surgery products can hospitals enquire about?

Accepted Answer

Hospitals can enquire about oxygenators, cardiopulmonary bypass accessories, tubing and related cardiac-surgery consumables. Availability and regulatory status vary by product and market.

Question 19

Which critical-care, ICU and OT products are available?

Accepted Answer

The catalogue covers categories such as ventilation, anaesthesia circuits, infusion products and surgical consumables. Ask for the current model list and technical documents.

Question 20

Do you manufacture medical devices?

Accepted Answer

Manufacturing, private-label and distribution status must be confirmed for each product. Request the legal manufacturer name and supporting documents before procurement.

Question 21

Do you offer OEM or private-label medical devices?

Accepted Answer

OEM enquiries are evaluated by product, specification, quantity, destination market and regulatory requirements. No OEM project should proceed without an agreed quality and regulatory plan.

Question 22

Can you export medical devices from India?

Accepted Answer

Export support can include product sourcing, document coordination and logistics. Actual eligibility depends on the product, destination-country registration, importer requirements and current trade rules.

Question 23

Which countries do you ship to?

Accepted Answer

Shipment feasibility is confirmed case by case based on product classification, carrier capability, destination regulations, import permits and distributor or hospital documentation.

Question 24

How do hospitals request a quotation?

Accepted Answer

Provide product name, manufacturer or acceptable equivalent, catalogue number, size, quantity, delivery location, required documents and target date through the contact page.

Question 25

What affects medical-device pricing?

Accepted Answer

Price can depend on model, size, quantity, shelf life, manufacturer, documentation, freight, insurance, taxes, currency and destination-market compliance.

Question 26

How can buyers verify product authenticity?

Accepted Answer

Check intact packaging, manufacturer details, catalogue and lot numbers, expiry, UDI where applicable, invoice chain, regulatory documentation and authorization with the manufacturer when required.

Question 27

How is product quality managed?

Accepted Answer

A robust process includes approved suppliers, incoming document checks, traceability, suitable storage, expiry control, packaging inspection and shipment records. Request product-specific evidence.

Question 28

Are all products CE marked or FDA approved?

Accepted Answer

Regulatory status is product- and market-specific. Do not assume a company-wide claim applies to every item; request the certificate, scope, model and issuing body for the exact product.

Question 29

How should sterile consumables be stored and shipped?

Accepted Answer

Follow label conditions and manufacturer instructions, protecting packages from moisture, heat, sunlight, crushing and temperature excursions. Cold-chain products require validated controls.

Question 30

How quickly can an order be delivered?

Accepted Answer

Lead time depends on stock, manufacturer schedule, documentation, payment, freight and customs. A written quotation should state the estimated dispatch and delivery window.

Question 31

Can procurement teams request samples or technical evaluations?

Accepted Answer

Sample or evaluation availability depends on the manufacturer, product classification and local rules. Clinical products must be handled under the appropriate institutional and regulatory controls.

Question 32

What information is needed for a product substitution?

Accepted Answer

Share the intended use, current catalogue number, dimensions, performance requirements, connector compatibility, regulatory needs and clinical constraints. Final equivalence must be assessed by qualified users.

Question 33

Does the website provide medical advice?

Accepted Answer

No. Website content is general educational and procurement information and does not replace instructions for use, institutional protocols or advice from qualified healthcare professionals.

Medical device and hospital supply FAQs