What are the opening hours?

Monday 08:00 - 17:00 Tuesday 08:00 - 17:00 Wednesday 08:00 - 17:00 Thursday 08:00 - 17:00 Friday 08:00 - 17:00

PT Mursmedic

Name: PT Mursmedic
Address: The Kensington Office Tower/11 Floor, Kelapa Gading/Jakarta, Jakarta, 14240, ID
Telephone: +622129078970

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PT Mursmedic

Mursmedic

27/08/2026

A Local Authorized Representative can play an important role in helping overseas manufacturers navigate local regulatory requirements and maintain compliance in their target market.

From regulatory communication and submission support to license maintenance and certain post-market responsibilities, the scope of local representation may continue beyond product registration.

Planning to expand into Southeast Asia? Connect with Mursmedic for local representation and regulatory support across the region.

26/08/2026

Meet Mursmedic Group at IMDEC 2026 in Kuala Lumpur, Malaysia.

Explore how Mursmedic Group supports healthcare companies across Southeast Asia through integrated market access solutions, including Independent License Holding & Importation, Product Registration, Regulatory & Quality Management Consulting, and B2B Distribution.

Visit us at MMDA Shared Booth 5137–5138 at the Kuala Lumpur Convention Centre (KLCC), Hall 5 from 26–28 August 2026. We look forward to connecting with you and discussing opportunities to support your healthcare expansion journey.

25/08/2026

On the occasion of Mawlid al-Nabi, may the teachings and exemplary character of Prophet Muhammad continue to guide us in fostering compassion, integrity, and care for one another.

May this celebration bring peace, blessings, and renewed purpose to all.

20/08/2026

Meet Mursmedic Group at the International Medical Device Exhibition & Conference in Kuala Lumpur, Malaysia, on 26–28 August 2026.

Visit us at MMDA Booth 5136 and connect with our team to explore our services across Southeast Asia, including Independent License Holding & Importation, Product Registration, Regulatory & Quality Management Consulting, and B2B Distribution.

We look forward to meeting you at the Kuala Lumpur Convention Centre.

19/08/2026

Malaysia’s Medical Device Authority (MDA) has transitioned the product classification application process to a fully online system, effective 1 August 2026. Applications must now be submitted through the designated Product Classification Application System, while approved classification letters will be issued directly by email.

For companies planning product classification or medical device registration in Malaysia, understanding the updated process is essential for smoother preparation.

Need support with regulatory or market access in Malaysia? Meet Mursmedic Malaysia at the Exclusive Business Matching Event and reserve your seat by scanning the QR code on the poster.

18/08/2026

Meet Mursmedic Malaysia at the Exclusive Business Matching Event hosted at the Embassy of the Republic of Indonesia in Kuala Lumpur on 27 August 2026.

Connect with our team and explore how Mursmedic Malaysia supports healthcare businesses through Independent License Holding & Importation, Product Registration, Regulatory & Quality Management Consulting, and B2B Distribution.

Reserve your seat by scanning the QR code in the poster and meet our team in Kuala Lumpur.

17/08/2026

Happy 81st Independence Day, Indonesia!✨

Celebrating decades of courage, unity, and progress. Let’s continue to embrace the spirit of independence, drive innovation, and build a better future together.

08/08/2026

Happy ASEAN Day 2026! 🌏✨

Mursmedic Group proudly supports hospitals, distributors, and healthcare innovation across Indonesia, Malaysia, Philippines, Singapore, Thailand, and Vietnam. Together, we continue advancing healthcare for better patient outcomes throughout the region.

💬 Consult with us about your healthcare needs or get in touch with our team today:
📧 [email protected]
📞 +62 811-1929-2933

30/07/2026

CDAKB, CPAKB, and ISO 13485 all support quality and compliance in the medical device industry, but each serves a different purpose. CDAKB focuses on distribution practices, CPAKB applies to medical device manufacturing in Indonesia, while ISO 13485 provides an international quality management system framework for organizations across the medical device lifecycle.

Understanding the difference helps companies identify the requirements that are most relevant to their activities and regulatory obligations. Need support in determining the right quality standard for your business?

Connect with Mursmedic for regulatory and quality compliance assistance.
📧 [email protected]
📞 +62 811-1929-2933
🌐 www.mursmedic.com
LinkedIn: PT Mursmedic

Address

The Kensington Office Tower/11 Floor, Kelapa Gading/Jakarta
Jakarta
14240

Opening Hours

Monday	08:00 - 17:00
Tuesday	08:00 - 17:00
Wednesday	08:00 - 17:00
Thursday	08:00 - 17:00
Friday	08:00 - 17:00

Telephone

+622129078970

Website

http://www.mursmedic.com/

Alerts

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