MEDICA 2026 | 16–19 November 2026 | Hall 6, Stall F37 | Düsseldorf, Germany
Precision-engineered single-use medical consumables certified to ISO 13485:2016 and CE standards, available for OEM procurement and bulk supply to Jakarta distributors.
The healthcare infrastructure of Greater Jakarta—comprising public apex institutions like RSUPN Dr. Cipto Mangunkusumo (RSCM), premier private hospital chains such as Siloam Hospitals and Hermina Hospital Group, alongside hundreds of specialized pediatric clinics—demands zero-compromise precision in intravenous therapy. In critical care environments, specifically Neonatal Intensive Care Units (NICU) and Pediatric Intensive Care Units (PICU), standard gravity infusion sets introduce unacceptable margin of error risks during drug administration.
A Measured Volume Burette Set (commonly referred to in Indonesian medical tender specifications as Infusion Set Burette 100ml / 150ml with Micro-Drip 60 Drops/mL) functions as an indispensable volumetric safeguard. It delivers precise micro-dosing of potent medication, electrolyte solutions, and parenteral nutrition, preventing fluid overload—a life-threatening risk in neonates and pediatric surgical patients.
Engineering excellence designed to prevent air embolism, maintain fluid accuracy, and eliminate contamination risks in intensive care settings.
Crystal-clear 100ml or 150ml burette chamber manufactured from high-impact medical-grade polycarbonate. Feature prominent, bold, micro-calibrated white/black graduation markings resistant to isopropyl alcohol wiping.
Integrated hydrophobic floating disk inside the burette base automatically seals the fluid outlet once the measured dose is fully delivered. This engineering feature completely prevents air entry into the fluid line, protecting patients against air embolisms.
Precision-moulded stainless-steel dropper needle calibrated to exactly 60 drops/mL ±5% delivery rate. Combined with a 15-micron fluid filter at the drip chamber bottom to intercept particulate matter prior to venous entry.
A side-by-side comparative analysis of clinical parameters for medical purchasing teams and hospital tender boards in Indonesia.
| Feature / Parameter | Measured Volume Burette Set (100ml / 150ml) | Standard Gravity IV Infusion Set | Micro-Drip Precision Infusion Line |
|---|---|---|---|
| Primary Target Patient | Pediatric, Neonatal, Oncology, ICU | Adult Medical-Surgical Wards | Pediatric General & Step-Down Wards |
| Chamber Capacity | 100 mL / 150 mL Cylindrical Burette | 10 mL – 20 mL Flexible Drip Chamber | 15 mL Rigid Micro Drip Chamber |
| Drip Calibration Factor | 60 Drops / mL (Micro-drip needle) | 20 Drops / mL (Macro-drip stem) | 60 Drops / mL |
| Safety Mechanisms | Auto Shut-Off Floating Valve + Air Vent Filter | Standard Roller Clamp (Manual control) | Roller Clamp + Micro-Slide Clamp |
| Material Formulation | DEHP-Free PVC / Medical Grade Polycarbonate | Standard Medical PVC / DEHP Optional | Phthalate-Free PVC / TPU Tubing |
| Injection Ports | Self-sealing Latex-Free Y-Site / Needle-Free Port | Latex / Latex-Free Flashbulb or Y-site | Needle-Free Valved Connector |
| Regulatory Standards | ISO 8536-5, ISO 13485, CE 2460 | ISO 8536-4, CE Certified | ISO 8536-4 / EN ISO 10993 |
For medical device importers, distributors, and tender winners operating out of Jakarta's central commercial hubs (such as Central Jakarta, West Jakarta, and the Tanjung Priok industrial corridor), sourcing directly from verified manufacturing facilities eliminates intermediary markups and guarantees batch traceability.
Lars Medicare operates an expansive manufacturing ecosystem in Sonepat (Haryana, India), equipped with ultra-modern Class 100,000 cleanrooms, fully automated high-speed assembly lines, and an independent ethylene-oxide (EtO) sterilisation chamber plant. Our internal infrastructure ensures every unit of Measured Volume Burette Set meets strict European Medical Devices Regulation (MDR) standards prior to export.
Comprehensive regulatory, technical, and commercial answers tailored to the Indonesian medical device procurement environment.
We provide a comprehensive regulatory dossier formatted for Indonesian AKL registration. This includes our ISO 13485:2016 certificate, CE Certificate of Conformity, Certificate of Free Sale (CFS) legalized by the relevant authority, full Product Technical Data Sheet, Biocompatibility Test Reports (ISO 10993 including cytotoxicity, sensitization, and systemic toxicity), Sterilisation Validation Reports (ISO 11135), and batch Certificate of Analysis (CoA).
DEHP (Di-2-ethylhexyl phthalate) is a plasticizer used to soften PVC. Clinical studies demonstrate that DEHP can leach out of infusion tubing into lipophilic drug solutions and blood components, posing potential endocrine and hepatotoxic risks to neonates, infants, and chemotherapy patients. Leading Jakarta hospital groups now mandate DEHP-free or Trioctyl Trimellitate (TOTM)-plasticized PVC compounds for all pediatric volumetric infusion devices.
From our Sonepat plant, consignments are dispatched via Nhava Sheva or Mundra sea ports. Transit time to Port of Tanjung Priok (Jakarta) typically ranges between 14 to 20 days. Production lead times for standard catalogue items are 3 to 4 weeks, whereas first-time private label OEM orders require 5 to 6 weeks to finalize custom pouch artwork, box printing, and sterilisation validation.
Yes. As a direct OEM manufacturer with an in-house tool room and moulding shop, we customize tubing length (standard 150cm / 180cm / 200cm), add extension lines, integrate needle-free split-septum access valves, incorporate rotating luer locks, or adapt specific drip chamber filter pore sizes (e.g., 1.2 micron or 5 micron fluid filters) according to hospital tender requirements.
For standard neutral-brand export packaging, orders can start from 1 mixed pallet (approx. 3,000–5,000 units). For customized OEM private label branding featuring your Indonesian company logo, Indonesian-language IFU (Petunjuk Penggunaan), customized box artwork, and UDI barcoding, the typical MOQ is 20,000 units per SKU to optimize printing and set-up economics.
The buoyant float valve rests at the bottom of the calibrated burette chamber. As long as liquid is present, the float remains suspended. Once the pre-measured liquid dose drains completely into the drip chamber, the float settles tightly into the elastomeric valve seat, creating an airtight seal. This stops the fluid flow instantly, preventing air from being sucked down the main tubing into the patient's peripheral or central vein.
Secure factory-direct pricing, certified ISO 13485 cleanroom quality, and complete regulatory registration assistance for your Jakarta medical device distribution business.
