Access verified product catalogues, clinical technical data sheets (TDS), ISO 13485 quality credentials, and regulatory compliance files for hospital procurement officers and global medical distributors.
Review comprehensive product dimensions, material biocompatibility summaries (ISO 10993), packaging configurations, and sterilisation release parameters across our complete range of medical disposables.
Comprehensive catalogue detailing over 400 SKUs across Renal Care, Urology, Infusion, Anaesthesia, Surgery, and Gastroenterology with complete product codes, French gauge (Fr) sizes, inner carton units, and master shipping specs.
Technical data sheets for Central Venous Catheter (CVC) Kits, Hemodialysis Catheters, Blood Tubing Sets, Peritoneal Dialysis Sets, and AV Fistula Needles, including polyurethane durability ratings and flow-rate performance benchmarks.
Engineering and material compliance data for Medical Infusion Sets, Blood Transfusion Sets, Safety IV Cannulae, Burette Sets, 3-Way Stopcocks, and Extension Lines with kink-resistant PVC and DEHP-free plasticizer options.
Dimensional matrices and balloon inflation pressure charts for 2-Way and 3-Way Silicone Coated Foley Catheters, Urine Collection Bags, Endotracheal Tubes, Tracheostomy Tubes, and Breathing Circuits.
Detailed technical sheets for Close Wound Suction Units, Chest Drainage Catheters, Biopsy Needles, Skin Staplers, Ryle's Tubes, and Levin's Tubes designed for operating theater precision and postoperative care.
Overview of ISO 13485 QMS certification, CE MDR technical files, ISO Class 7/8 Cleanroom bioburden protocols, Ethylene Oxide (EO) sterilization residue testing records, and Free Sale Certificates for tender registration.
With over three decades of medical device manufacturing experience in Vatva, Ahmedabad, Shree Umiya Surgical Pvt. Ltd. provides complete traceability, stringent batch testing, and reliable global tender support.
Our manufacturing plant operates under controlled environment conditions to guarantee patient safety and zero clinical failure rates.
We support global importers and medical brands with private label manufacturing solutions tailored to regional MOH guidelines.
Find direct answers regarding documentation, product testing data, certificate requests, and tender sample dispatch.
Every export shipment from Mediplus includes a lot-specific Certificate of Analysis (CoA), Sterilization Release Certificate, and Material Compliance Declaration. If you require additional copies for regulatory auditing, contact our quality assurance team with your lot or invoice number.
Yes. Biocompatibility data summaries conducted in accordance with ISO 10993 standards (Cytotoxicity, Sensitization, Irritation, Hemocompatibility, and Systemic Toxicity) are available for registration holders and official distribution partners.
Our engineering and regulatory divisions regularly customize product length, lumen configuration, connector type (Luer Lock / Luer Slip), needle gauge, and packaging formats to match strict government tender specifications across international health authorities.
Evaluation sample kits complete with technical datasheets and sterilisation indicators can be dispatched to registered distributors, hospital chains, and procurement offices upon verification of company credentials.
Connect directly with our regulatory specialists and export engineering team to receive custom product technical files, private-label quotation estimates, or evaluation sample packs.
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