Disposable IV Infusion Set With Burette

Disposable IV Infusion Set With Burette

Disposable gravity‑operated IV infusion set with burette, volume‑limited chamber minimises fluid‑over‑infusion risks for paediatric, elderly and critical‑care patients. CE & ISO13485 certified, free samples and customisable configurations for medical distributors.
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Description
Technical Parameters

Product Information

01 Disposable Infusion Set - Volume‑Bound Gravity Infusion Solution

Standard gravity IV sets cannot cap total delivered fluid volume, which creates safety hazards for vulnerable patient groups. Our burette‑equipped infusion set addresses this gap by adding a standalone graduated measuring chamber. Clinicians pre‑load only the intended fluid dosage inside the transparent burette before starting infusion, limiting maximum possible fluid intake and lowering risks of accidental volume overload.

This EO‑sterile single‑use assembly works purely on gravity power. It combines graduated measuring unit, drip‑viewing section, flow‑adjustment roller and long flexible tubing into one complete kit. Widely deployed in paediatric wards, geriatric units, emergency departments and critical‑care settings.

 

02 Product Specifications

Item Details
Operating Principle Gravity‑powered intravenous infusion with pre‑measured burette chamber
Standard Tubing Length 150 cm
Burette Available Capacity 100ml, 150ml
Needle 21-25G
Connector  Luer Slip, Luer Lock
Sterilization EO gas, single‑patient use only
Shelf  Life 5 Years
Certificates CE, ISO13485
Package

1pc/PE bag, 5pcs/bag, 100pcs/ctn;

B2B Support Free evaluation samples, OEM / ODM customisable

 

03 Core Working Modules (practical‑use perspective)

  • Graduated transparent burette measuring chamber: Clear milliliter scale enables direct visual reading. Available capacities from 100 ml, 150 ml. Healthcare staff fill exact prescribed volume inside this chamber ahead of infusion.
  • Integrated drip‑view chamber: Dual function: observe dripping frequency to calculate real‑time drip rate; trap air bubbles to help avoid air‑embolism risks entering patient's venous circulation.
  • Roller‑style flow adjuster: Stepless adjustment to speed‑up or slow‑down drip speed to satisfy different treatment requirements.
  • Kink‑resistant long medical tubing: Tolerates patient position shifts without blocking liquid flow; compatible with peripheral IV cannulas, central venous catheters and winged butterfly needles.
  • Full connection assembly: Piercing spike for hanging fluid containers plus patient‑end connector ready to pair with mainstream venous‑access hardware.

 

04 Where This Burette Infusion Set Adds Real Clinical Value

Scenarios that demand hard volume limits for IV delivery:

  • Paediatric and elderly patient infusion where even minor fluid excess brings safety risks
  • Critical‑care cases requiring close volume tracking during fluid resuscitation
  • IV delivery of pharmaceuticals with narrow safe‑dosage therapeutic window
  • Controlled‑dose parenteral nutrition and electrolyte correction
  • Regulated‑volume transfusion of blood‑derived products

 

05 Hands-On Clinical Operational Tips

  • For single‑patient use only. Do not reuse whole set or separate components to prevent cross‑infection.
  • Complete full air‑bubble purging inside burette, drip‑chamber and tubing before you hook‑up to patient venous access.
  • Continuously keep eyes on burette scale and drip‑rate status through the full infusion cycle, tweak flow speed following patient condition.
  • Once procedure completes, discard entire assembly into dedicated medical‑waste receptacle, do not take apart for reuse.
  • Never deploy if individual sterile pouch shows tearing, punctures or broken seals.

 

06 Manufacturing & B2B Procurement Information

DJI0868

Production takes place inside ISO13485‑compliant clean‑room facilities. Every production batch goes through multi‑level validation: incoming raw‑material audit, component dimensional & functional testing, sterilisation‑cycle validation plus finished‑product sampling inspection prior to shipment.

We cater for import traders, government procurement projects and medical‑chain‑store buyers. Customisable items cover burette chamber capacity selection, tubing length, connector variant, accessory configuration, outer carton printing and labelling requirements. Reach sales team to discuss project‑specific needs and get sample support.

 

Quality & B2B Supply

Produced within ISO13485 certified clean‑room workshops. Each batch passes raw‑material check, component function testing and sterilization validation. Customisable items include connector style, needle gauge, volume and outer carton printing. Contact sales for bulk pricing and sample requests.

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Worker operation
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Automated production line
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Clean workshop

Certificates

TUV SUD ISO 2025 E_01(1).png
ISO 13485
Chengwumedical CE Certificate TUV-Blood Collection Needle IV Giving_01(1).png
CE

 

 

We are Here for You

write to us
Email
sales18@chengwumedical.com
visiting us
Address
Room 1802, West Tower, Gome Smart City, Guangzhou City, Guangdong Province
WhatsApp
Number
+86 18406615801
Contact directly
Phone
+86 18406615801

 

FAQ

Q1: When should burette‑fitted infusion set replace regular standard IV sets?

A: Pick burette‑equipped models when you need physical volume capping. It shines for children, seniors, critical‑care subjects or narrow‑margin‑dosage drugs, to guard against fluid overload. Conventional IV kits lack this pre‑measurement feature.

Q2: Can we visit your company?

A: Absolutely! You are very welcome to visit us.

Q3: What compliance‑related documentation can you furnish for import‑registration and customs‑clearance?

A: CE and ISO13485 certification files can be delivered upon business‑party request.

Q4: Can you offer OEM / ODM service?

A: Yes. We support OEM services including custom printed boxes, private labels and customized packing specifications. MOQ applies.

Q5: What is the lead time for bulk orders?

A: Normally 30–45 days after receiving your deposit. Lead time will be confirmed according to order quantity and packaging requirements.

 

 

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