Sterile single-use medical disposables manufactured by Mediplus India
Manufacturer & Exporter Since 1988

Medical Disposables Engineered For Clinical Confidence

Single-use devices for dialysis, infusion, urology, anaesthesia and surgery — produced in ISO 13485 clean-room lines in Ahmedabad, India.

Central venous access and haemodialysis catheter kits for renal care
Renal Care Portfolio

Dialysis & Vascular Access Solutions

CVC kits, haemodialysis catheters, blood tubing and AV fistula needles validated batch by batch.

Quality controlled clean room production of disposable medical devices
Quality You Can Audit

ISO 13485 & CE Certified Production

Validated EO and gamma sterilisation, full traceability and export documentation with every shipment.

Medical disposables exported to hospital distributors worldwide
Global Distributor Support

OEM & Private Label Programmes

Your brand, our validated production lines — artwork, IFUs, UDI and registration dossiers handled in-house.

ISO 13485QMS & CE marked device families
70+ CountriesDistributor & tender supply network
36+ YearsManufacturing experience since 1988
400+ SKUsAcross 7 clinical specialities
Why Procurement Teams Choose Mediplus

Evidence-Backed Manufacturing, Not Just Catalogue Pricing

Everything a hospital buyer, importer or tender agent needs to qualify a supplier — documented, verifiable and shipped on schedule.

Regulatory & Quality Assurance Dossier

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Our regulatory team maintains live technical files so your registration submission does not wait on the factory.

  • ISO 13485 / ISO 9001 certified quality management system
  • CE marked device families with technical documentation
  • Free Sale Certificate, CoA and sterilisation release records per batch
  • Biocompatibility (ISO 10993) and stability data summaries

Export Logistics & OEM Programmes

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From a single mixed container to repeat annual tender volumes, order handling is managed by one dedicated export desk.

  • Private-label artwork, multilingual IFU and UDI/barcode support
  • 3–4 week lead time on catalogue items after order confirmation
  • FOB / CIF / CFR shipping from Mundra & Nhava Sheva ports
  • Container-optimised cartons to reduce freight cost per unit
Product Categories

Seven Clinical Ranges of Single-Use Medical Devices

Browse by department to match your hospital, dialysis centre or wholesale requirement with the right Mediplus range.

Featured Products

High-Demand Disposables From Our Export Range

Frequently reordered SKUs by dialysis chains, group purchasing organisations and government tender buyers.

Browse All Products
About Mediplus India

Healthcare For All Mankind — Manufactured In Ahmedabad Since 1988

Shree Umiya Surgical Pvt. Ltd. (SUSPL), known globally under the Mediplus brand, began manufacturing single-use medical disposable devices in 1988 at Vatva, Ahmedabad, Gujarat. Three decades of continuous process refinement allow our brands to stand alongside leading international labels on quality, while volume production keeps our landed cost competitive for importers.

Every device leaving our plant is traceable to its raw-material lot, moulding shift, assembly clean room and sterilisation cycle. That traceability — not marketing claims — is what has kept distributors, dialysis networks and public-health tender buyers reordering from us for years.

1988Established
70+Export Markets
7Clinical Divisions
100%Single-Use Devices
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Mediplus India manufacturing facility with rooftop solar power installation
Infrastructure & Process Control

How A Mediplus Device Is Built, Checked And Released

Our vertically integrated plant covers granule-to-carton production, which removes the quality variability that comes with outsourced sub-assembly.

  • Medical-grade raw material intake: PVC, PU, silicone and latex lots verified against supplier CoA before release to the floor.
  • In-house moulding & extrusion: injection moulding and tube extrusion under controlled parameters for dimensional consistency.
  • Clean-room assembly: ISO Class 7/8 rooms with gowning protocol, differential pressure and particle monitoring.
  • Validated sterilisation: ethylene oxide or gamma irradiation with biological indicator and EO-residue release.
  • Final QC & documentation: leak, tensile, flow-rate and package-integrity testing before batch certification.
  • Sustainable operations: rooftop solar generation reduces the carbon footprint of every unit produced.
Explore Our Infrastructure
Meet Us Worldwide

Upcoming International Medical Exhibitions

Inspect samples, discuss OEM specifications and review documentation with our export team in person.

2026
17 – 19 June
WHX Miami 2026 healthcare exhibition logo

WHX Miami

Miami Beach Convention Centre, Miami, USA

Stand No. E-24
2026
17 – 19 September
Medical Fair India 2026 exhibition logo

Medical Fair India

Hall 4, Bombay Exhibition Centre, Goregaon (E), Mumbai, India

Stand No. E-50
2026
16 – 19 November
MEDICA Dusseldorf 2026 trade fair logo

MEDICA

Messe Dusseldorf, Germany

Appointments open
2027
25 – 28 January
WHX Dubai Arab Health 2027 exhibition logo

WHX Dubai (Arab Health)

Dubai Exhibition Centre, Dubai, UAE

Appointments open
Buyer FAQ

Sourcing Questions Answered By Our Regulatory & Export Team

Practical answers to the questions importers, tender consultants and hospital buyers ask us most often.

Our Vatva, Ahmedabad plant operates a quality management system certified to ISO 13485 and ISO 9001, with CE marked product families under the EU MDR pathway and production in ISO Class 7/8 clean rooms. Batch-wise documentation, sterilisation validation records and Certificates of Analysis accompany every export consignment, and our facility is open to customer and notified-body audits.

Yes. We produce private-label infusion sets, catheters, dialysis lines and anaesthesia consumables with buyer-specified artwork, multilingual IFUs, carton dimensions, barcodes and UDI data. Artwork proofing usually takes 5–7 working days, followed by a pilot batch for your approval before mass production.

Standard catalogue items typically start at one pallet per SKU, while private-label programmes begin at a single 20-ft container with a mixed SKU load. Regular items ship in 3–4 weeks; new OEM tooling or registration-linked items require 6–8 weeks from artwork approval. Shipments move via Mundra and Nhava Sheva on FOB, CIF or CFR terms.

Single-use devices are sterilised by ethylene oxide (EO) or gamma irradiation depending on material and design. Each cycle is released against biological and chemical indicators, EO residue limits and bioburden testing. Validation dossiers and shelf-life data are shared with registration holders and notified bodies on request.

Our regulatory team supplies Free Sale Certificates, ISO 13485 and CE certificates, technical files, biocompatibility (ISO 10993) summaries, stability data and legalised or apostilled documents required by Ministries of Health across the Middle East, Africa, Latin America, CIS and Southeast Asia. Country-specific formats can be prepared on request.

Share your SKU list, sizes, annual quantity and destination port through our enquiry page or write to [email protected]. Specification sheets, packing data and catalogue PDFs are also available on the downloads section for immediate reference.

Products

Seven clinical ranges, 400+ single-use device SKUs.

Downloads

Catalogue, product sheets and certificate references.

Achievements

Recognitions, approvals and export milestones.

Support

Technical, regulatory and after-sales assistance.