Sales: +91 9099 928 652 [email protected] Mon – Sat : 10:00 AM – 07:00 PM (IST)

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Direct Global Sales, OEM Contract Manufacturing & Technical Support Desk

Global Export Communication

Direct Business Channels for Overseas Buyers

Our specialized international export desk responds to inquiries from medical device distributors, procurement officers, hospital networks, and CDMO partners within 24 business hours.

Factory & Head Office

  • Angiplast Private Limited
  • Survey No. 589/1, 590, Village Vasana Buzarg, Dholka Road, Kheda, Gujarat, India - 387411

Export & Sales Hotline

  • Sales Desk: +91 9099 928 652
  • Export Desk: +91 9099 930 560
  • General Hotline: +91 9662 004 148 / 149

Official Corporate Email

Business Support Hours

  • Monday – Saturday
  • 10:00 AM – 07:00 PM (IST)
  • Time Zone: GMT +5:30
Enterprise & B2B Assistance

Dedicated Departmental Support for Global Partners

Whether you require tender bid documentation, validated cleanroom assembly details, or OEM product customisation, our qualified engineers and regulatory affairs experts are ready to assist.

International Tenders & Bulk Procurement

Our specialized export team works closely with government ministry health tenders, international purchasing groups, and regional importers across 52+ countries. We provide verified technical dossiers, notarized Free Sale Certificates (FSC), ISO 13485 compliance files, and consolidated sea/air freight logistics management.

  • Customs & shipping documentation for smooth clearing
  • Multilingual pouch artwork & localized packaging
  • Container load optimization (FCL / LCL shipments)

CDMO & OEM Contract Manufacturing Desk

Partner with Angiplast for custom injection moulding, extrusion line setup, and specialized private-label device production. Operating Class 10,000 cleanrooms and in-house ETO sterilisation, we assist global medical brands from initial drawing review to full batch validation.

  • In-house tool room for rapid prototype development
  • Needle-free valve lines & custom respiratory assemblies
  • Lot-level traceability and cleanroom bioburden reporting
Export Reliability Assurance

Rigorous Standards for International Compliance

When sourcing single-use medical devices, overseas buyers need guaranteed traceability, compliance certification, and batch consistency. Angiplast operates strictly under ISO 13485 QMS guidelines, backed by international CE certification and US FDA 510(k) clearances on selected product lines.

Our in-house quality control laboratory performs biological, physical, and chemical testing for every production run, ensuring complete compliance before release.

  • 100% in-house moulding, assembly, printing, and ETO sterilisation
  • Batch-specific sterility release and residual ETO testing verification
  • Complete regulatory submission support for product registration in your destination country
Angiplast ISO 13485 cleanroom production quality verification ISO 13485 • CE Certified Plant

Connect with Our International Export Team Today

Discuss your product specifications, request sample units, or receive comprehensive technical file documentation directly from our export sales division.

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