ISO 9001 & ISO 13485 Certified WHO-GMP CE Marked Manufacturing in India since 1955
Contact Sterimed Group Global Sales Desk
Global Trade & Export Division

Contact Us

Connect directly with Sterimed Group's international sales engineers, OEM product specialists, and regulatory dossier support team.

Direct Manufacturer Communication

Get in Touch with Sterimed Group Export Operations

Whether you are an international healthcare distributor, medical device importer, hospital procurement group, or OEM brand partner, our dedicated export department provides technical consultation, batch availability, competitive CIF/FOB pricing, and full regulatory dossier documentation.

Corporate Headquarters

Sterimed Medical Devices Pvt. Ltd.

Sterimed Surgicals (India) Pvt. Ltd.

Registered Office Address

501, Ring Road Mall, Manglam Place, Sector-3, Rohini,
New Delhi - 110085, India

Direct Communication Lines

International Export Desk Email: [email protected]

Domestic Sales & Inquiries Email: [email protected]

Telephone Hotline: +91-11-48880000 / +91-11-42466196 (100 Lines)

Working Hours: Monday – Saturday: 09:30 AM – 06:30 PM (IST / UTC+5:30)

Dedicated Buyer Support

Services for Overseas Buyers & Importers

Sterimed Group serves medical device partners across 90+ countries with structured export execution and technical transparency:

  • OEM & Private-Label Packaging: Custom artwork, multilingual IFUs, barcoding, and market-specific compliance labels.
  • Regulatory Dossier Assistance: Technical files, ISO 13485 QMS documentation, CE declarations, WHO-GMP certificates, and Free Sale Certificates (FSC).
  • Evaluation Samples: Fast-track physical sample dispatch for clinical trial and hospital evaluation committees.
  • Quality Traceability: Complete batch-wise sterility validation reports, EO residual limits, and material certificates for every container shipment.
Manufacturing Excellence

Why International Healthcare Purchasing Teams Choose Sterimed

65+ years of continuous manufacturing tradition combined with automated cleanroom production lines.

Global Certification Compliance

Operates under audited ISO 13485:2016 and ISO 9001 quality management systems. All device ranges carry validated CE documentation and WHO-GMP compliance.

High-Volume Production Capacity

Equipped with high-capacity extrusion, dipping, molding, and Ethylene Oxide (EO) sterilization chambers to ensure stable supply chains for large-scale national tenders.

End-to-End Traceability

Every single product pouch and shipping carton is stamped with clear lot numbers, production timestamps, sterilization indicators, and expiration dates.

Procurement FAQ

Frequently Asked Questions by International Buyers

Our dedicated international sales team responds to all tender inquiries, RFQs, and product documentation requests within 24 business hours.

Yes. We provide complete technical files, Certificates of Free Sale, ISO 13485 certificates, CE documentation, and test reports required for medical device registration in LATAM, EMEA, Southeast Asia, and Africa.

We offer FOB, CIF, CFR, and EXW shipping terms. Standard packaging options include sterile individual pouches, inner boxes, and export-grade heavy-duty corrugated shipping cartons.

Ready to Partner with a Trusted Medical Disposables Manufacturer?

Click below to send your technical inquiry, request sample kits, or initiate tender quotes with our global export desk.

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