Engineered for continuous hourly diuresis measurement, strict CAUTI prevention, and high-acuity ICU renal monitoring. Supplied to hospital networks and brand owners across 52+ countries.
Integrated hydrophobic bacterial vents and dual anti-reflux valves engineered to eliminate retrograde contamination risks and protect ICU patients.
Dual or triple-chambered 200ml / 500ml rigid meters with crystal-clear micro-graduations for exact low-volume hourly renal fluid balancing.
In-house injection moulding, clean room assembly, and ETO sterilisation supporting custom graduations, tubing lengths, and private labels.
In intensive care units (ICU), surgical recovery, trauma wards, and renal therapy centers, accurate monitoring of hourly urinary output is a vital surrogate indicator of cardiac output, systemic organ perfusion, and acute kidney injury (AKI) onset. A standard urine bag lacks the volumetric resolution necessary to register low hourly outputs (such as oliguria where output drops below 0.5 mL/kg/h). To address this critical diagnostic requirement, medical device purchasers, hospital procurement officers, and medical brand owners turn to specialized Urinemeter with Drain Bag systems.
A precision Urinemeter with Drain Bag combines a rigid, clear, micro-graduated measuring chamber (urinemeter) directly interfaced with a flexible, high-capacity collection reservoir (drain bag). This closed system design allows intensive care nurses to record exact hourly urine flow—even down to 1 mL increments—before tilting the chamber to transfer the measured fluid into the primary 2000 mL or 2600 mL drainage bag. Beyond volumetric precision, modern procurement tenders prioritize advanced infection prevention mechanisms designed to combat Catheter-Associated Urinary Tract Infections (CAUTI), which account for a substantial percentage of healthcare-associated infections worldwide.
When sourcing a Urinemeter with Drain Bag for public healthcare tenders or private hospital systems, evaluating price alone is insufficient. Procurement teams must scrutinize the hydrophobic air filter porosity, needleless sampling port seal integrity, anti-reflux mechanism design, polymer biocompatibility (DEHP-free compliance), and the manufacturer's validated Ethylene Oxide (ETO) sterilisation sterility assurance level (SAL 10-6).
Angiplast Private Limited manufactures closed-system Urinemeters engineered to fulfill rigorous international medical standards including ISO 8669 (Urine collection bags) and ISO 13485 quality management guidelines. Below is an exhaustive technical review of the anatomical components that comprise our premium urology range.
Constructed from optical-grade, shatter-resistant rigid polystyrene or polypropylene, the measuring chamber is calibrated with bold, indelible graduations. It features a multi-chamber design (e.g., a 50 mL inner micro-measuring section within a 200 mL or 500 mL primary chamber) ensuring precise readings for both pediatric and adult critical care patients.
Manufactured from high-transparency, medical-grade polyvinyl chloride (PVC) with high-frequency welded seams that withstand burst pressure test thresholds exceeding standard clinical requirements.
Class 10,000 Cleanroom Assembled | Parameter | ICU / Critical Care Standard Model | Pediatric / Low-Volume Precision Model | High-Capacity Operating Room Model |
|---|---|---|---|
| Chamber Capacity | 500 mL (Dual / Triple Chamber) | 200 mL (Micro-graduated Inner Burette) | 500 mL Burette + Extra Venting |
| Drain Bag Capacity | 2000 mL / 2500 mL | 1000 mL / 2000 mL | 2600 mL / 3000 mL |
| Tubing Dimensions | 120 cm ID: 7.0 mm, OD: 10.0 mm | 120 cm Kink-Resistant PVC | 150 cm Extra-Wide Bore Tubing |
| Sampling Mechanism | Self-sealing needleless port | Needleless / Needle port option | Swabable needleless valve port |
| Sterilisation Method | Ethylene Oxide (ETO) gas (Sterile) | Ethylene Oxide (ETO) gas (Sterile) | Ethylene Oxide (ETO) gas (Sterile) |
| Compliance & Material | Medical Grade PVC (DEHP-Free available), ISO 10993 compliant | Biocompatible Polymer, ISO 10993 certified | Phthalate-Free options, CE MDR Class IIa ready |
Choosing the correct product variant ensures optimal clinical performance and cost efficiency for healthcare institutions. Below are our core product recommendations based on departmental requirements.
Best For: Adult Intensive Care Units, Cardiac Surgery Recovery, Trauma Centers.
Features dual-chamber volumetric resolution, needleless aspiration port, hydrophobic anti-microbial air vent, and rigid twin-hook hanger. Provides maximum nurse safety and acute diuresis precision.
Best For: Neonatal ICU (NICU), Pediatric ICU, Specialized Renal Clinics.
Equipped with a 200ml chamber featuring fine 1ml graduation increments up to 40ml. Prevents measurement rounding errors in neonates and low-weight infants requiring exact fluid balancing.
Best For: Long-duration operating room procedures, post-operative surgical wards.
Combines a 500ml rigid meter with a 2600ml or 3000ml heavy-duty drainage reservoir. Features rapid-drain T-tap valves and extra-long wide-bore tubing to handle high-volume perioperative urine flow.
As healthcare purchasing shifts from fragmented transactional ordering to centralized, risk-mitigated supply chain partnerships, several macroeconomic and clinical trends are shaping global demand for Urinemeter with Drain Bag products:
Hospitals are replacing open or semi-closed drainage bags with strict closed-system urinemeters that feature needleless sampling ports and non-touch emptying valves. Procurement contracts increasingly mandate documented CAUTI risk mitigation data from suppliers.
Regulatory authorities in the EU (under MDR 2017/745) and North America are heavily restricting DEHP plasticizers in long-term catheterization disposables. Supply chains are transitioning to alternative non-phthalate plasticizers (e.g., TOTM, DINCH) and bio-compatible medical polymers.
While mechanical urinemeters remain the global clinical standard, future developments point toward optical sensor attachments and automated diuresis tracking interfaces. Forward-thinking manufacturers are designing rigid chambers with standard geometry compatible with digital monitoring docks.
Global distributors and hospital networks are actively diversifying sourcing away from single-country dependence. India—and specifically established manufacturers like Angiplast Pvt. Ltd.—has emerged as the premier hub for high-volume, ISO 13485-certified single-use medical disposables with reliable lead times.
Founded in 1994 in Kheda / Ahmedabad, Gujarat, Angiplast Private Limited has built a worldwide reputation as a premier OEM/CDMO manufacturer and exporter of single-use medical disposables. Here is why international buyers choose Angiplast for high-stakes urology requirements.
Established 1994 · Exporting Worldwide Answers to technical, regulatory, and logistics questions asked by international healthcare buyers, hospital tenders, and OEM partners.
Catheter-Associated Urinary Tract Infections (CAUTI) occur when bacteria migrate retrograde into the urinary tract. Angiplast Urinemeters incorporate a multi-layer defense strategy: (1) A true closed system where the meter and bag remain permanently connected, eliminating air-path exposure; (2) Dual anti-reflux valves located at the catheter inlet and chamber outlet to prevent urine backflow; (3) A needleless, self-sealing sampling port that eliminates needle punctures and external pathogen entry; and (4) Hydrophobic micro-porous air vents on both the measuring chamber and drainage bag that prevent vacuum lock while blocking bacterial migration.
Our Urinemeters are engineered with a dual-chamber design. The inner micro-chamber measures low urine volumes from 1 mL up to 40 mL with a high-precision tolerance of ±1 mL. For higher volumes, the outer chamber measures up to 500 mL in 5 mL and 10 mL graduations. The high optical clarity of our medical-grade polystyrene ensures nursing staff can record exact hourly readings without parallax errors.
Yes. In full compliance with European Union Medical Device Regulation (EU MDR) guidelines and global environmental standards, Angiplast offers DEHP-free and phthalate-free PVC tubing and bag formulations. Biocompatibility testing is conducted in accordance with ISO 10993 standards for cytotoxicity, systemic toxicity, and hemocompatibility.
Angiplast Urinemeter with Drain Bag systems have a validated 5-year shelf life when stored in original, undamaged blister/pouch packaging. Sterilisation is conducted in our captive Ethylene Oxide (ETO) plant using validated cycles according to ISO 11135 standards. Each production batch undergoes biological indicator testing, bioburden testing, and residual ETO analysis (ISO 10993-7) prior to QA release.
For standard Angiplast brand packaging, MOQs start as low as 1,000 units depending on regional distribution terms. For OEM, private-label artwork, customized graduation printing, or specific tubing configurations, MOQ typically starts at 5,000 to 10,000 units per batch to optimize cleanroom setup and printing runs.
Absolutley. Our regulatory affairs team provides complete technical documentation packs including ISO 13485 certificates, CE certificates, Free Sale Certificates (FSC) issued by Indian FDA authorities, Declaration of Conformity, Device Master Files (DMF), biological safety reports, and stability test summaries to support registration with local Ministries of Health worldwide.
We provide three primary outlet valve options based on clinical preference and tender requirements: (1) T-Tap Valve for fast, one-handed splash-free emptying; (2) Lever Tap Valve for smooth rotational control; and (3) Twist Drain Valve for traditional low-profile drainage. All valves are 100% pressure-tested against leaks during assembly.
Partner with an ISO 13485 certified manufacturer for precision Urinemeter with Drain Bag systems. Request technical datasheets, factory audit reports, or custom OEM quotes instantly.
