
0~1100 Ml, Error ± 1% or 1ml Urine Flow Meter Uroflowmetry with ISO13485

CE Approved 0~1100 Ml, Error ± 1% or 1ml Urine Flow Meter Portable Uroflowmetry

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When sourcing urine meters, prioritize models with a dual-chamber design (a small precision chamber for low volumes and a larger bag for total output). Ensure the device features a needleless sampling port to prevent needle-stick injuries and a hydrophobic filter to prevent retrograde infection. The graduation markings must be clear, indelible, and accurate to ±5% for clinical precision.
As a Class II medical device, urine meters must comply with ISO 13485 (Quality Management Systems for Medical Devices). For the US market, FDA 510(k) clearance is required, while the EU market necessitates CE Marking (MDR 2017/745). Additionally, verify that the product is EO (Ethylene Oxide) sterilized and meets ISO 10993 standards for biocompatibility.
Check for a built-in anti-reflux valve that prevents urine from flowing back into the drainage tube, which is critical for reducing Catheter-Associated Urinary Tract Infections (CAUTI). Request the supplier to provide validation reports for microbial barrier integrity and ensure the drainage tap is designed for one-handed, aseptic operation.
The collection bag should be made of medical-grade PVC with a thickness of at least 0.12mm to 0.15mm to prevent leakage. For patients with sensitivities, consider sourcing DEHP-free or Latex-free components. The tubing should be kink-resistant to ensure continuous flow even when the patient moves.
Never skip the pre-shipment inspection (PSI). Hire a third-party agency to perform a leakage test and sterility seal integrity check on a random sample (AQL 1.0 or 1.5). Ensure the supplier provides a Certificate of Analysis (CoA) for every batch and verify their presence on Made-in-China.com to check their audited supplier status.
Medical supplies often face stricter customs scrutiny. Negotiate for FOB or CIF terms where the supplier handles export clearance. Ensure the remaining shelf life of the sterile products is at least 80% of the total duration upon arrival. For shipping, use temperature-controlled environments if the plastic components are prone to degradation in extreme heat.
Utilize Escrow services or Letters of Credit (L/C) for large-scale orders to ensure funds are only released upon verification of shipping documents. When sourcing via Made-in-China.com, prioritize Diamond Members or Audited Suppliers who have undergone comprehensive on-site verification by independent bodies like SGS or TÜV Rheinland.
Prepare a comprehensive document package including the Commercial Invoice, Packing List, Bill of Lading, and Certificate of Origin. Specifically for urine meters, you must include the Declaration of Conformity, Sterilization Certificate, and the Product Registration Certificate relevant to your local health authority (e.g., MHRA, TGA, or Health Canada).