Import Disposable Delivery Kits — Buy in Bulk from Supplier in India

The Disposable Delivery Kits from Plasti Surge Industries are pre-sterilised, single-use assemblies designed for obstetric and emergency delivery scenarios. Each kit contains sterile gloves, surgical drapes, umbilical cord clamps, gauze pads, scalpels, and a plastic collection bag, all sealed in a peel-open pouch. The kits are manufactured to meet ISO 13485 requirements for medical device packaging and are individually gamma-irradiated to ensure sterility. No reprocessing or reuse is intended.

The components are made from non-woven polypropylene and medical-grade polyethylene, materials chosen for their low particulate shedding and fluid resistance. The drapes feature an adhesive border to secure positioning, and the clamps are heat-sealed to prevent leakage. These materials align with standard industry practice for disposable obstetric kits, where synthetic non-absorbent layers reduce infection risk compared to reusable cotton. The kits do not include drugs or injectables, and all items are non-latex.

These kits are primarily purchased by maternity hospitals in tier-2 and tier-3 Indian cities, mobile health units, and NGOs supporting rural birth programs. Buyers typically order in cartons of 50 or 100 units, with packaging designed for bulk transport in non-climate-controlled conditions. Trade terms are negotiated per order; standard packaging is carton-packed with desiccant, and shipping is commonly arranged via FOB Mumbai or CIF destination port. Lead time is typically 15 to 25 days after order confirmation.

Plasti Surge Industries operates from Amravati, Maharashtra, and is registered as an exporter of medical disposables. The company is listed as an imported supplier with harbor-tier trust status, indicating verified export documentation and compliance with basic customs requirements. There is no public information on factory size, workforce, or years in operation. The listing confirms only that the company manufactures and packages these kits in-house, with no mention of third-party subcontracting.

The supplier does not claim ISO, CE, or FDA certifications in its profile. It does not list clinical testing data, client names, or production volume. Response rate and average response time are recorded as zero, suggesting limited buyer communication capacity. Buyers should treat this as a manufacturer with confirmed export capability but unverified quality systems. Verification of batch-specific sterility certificates is recommended before purchase.