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MEDICAL DEVICE AUTHORITY (MDA) REGULATORY INFORMATION SUBSCRIPTION

INTRODUCTION

 This program of e-mail notification subscription is an initiative of MDA to provide the latest information to stakeholders and general public who wish to subscribe to this service. This is one of the initiatives that MDA is offering to promote effective dissemination of information to individuals and companies that values on time and direct access to pertinent regulatory information and activities related to medical devices.

OBJECTIVE

  • MDA publishes/ issues new regulatory information on medical device; and
  • With this program, updated pertinent information from MDA is directly accessible to the stakeholders such information are including but not limited to the following:
  1. Gazettement orders;
  2. Regulations;
  3. Policies;
  4. Guidance documents;
  5. Guidelines;
  6. Programs;
  7. Trainings; and
  8. Others related to regulatory information.

WHO HAS TO SUBSCRIBE

The target group for the implementation of MDA e-mail notification subscription is as follows:

  • Manufacturers, authorized representatives, importers, and distributors;
  • Conformity Assessment Bodies (CABs);
  • Medical device associations;
  • Healthcare institutions or universities;
  • Healthcare professionals (HCPs);
  • Testing labs;
  • Students; and
  • Interested individual.

HOW TO SUBSCRIBE

Applicants shall apply and submit an application fee to the MDA.

Only pertinent relevant information will be required. The application process consists of five main steps, namely:

 

Step 1 : Click on the Application Form to subscribe/ unsubscribe E-mail subscription.

Step 2 : Fill in all required information and ensure all information entered are

              correct.

Step 3 : Submit completed Application Form by clicking on the submit button.

Step 4 : Tax invoice will be issued MDA to the applicant via email supplied in the application form.

Step 5 : All applications will be charged RM 100 per application. The validity of e-mail notification subscription is valid for one (1) year. The subscriber will receive an e-mail reminder 30 days before the expiration date for renewal. Payment shall be made through bank draft, payable to:

"KUMPULAN WANG PIHAK BERKUASA PERANTI PERUBATAN" and courier to;

KETUA EKSEKUTIF

PIHAK BERKUASA PERANTI PERUBATAN,

KEMENTERIAN KESIHATAN MALAYSIA, ARAS 6, PRIMA 9, PRIMA AVENUE II, BLOCK 3547, PERSIARAN APEC, 63000 CYBERJAYA, SELANGOR.

Note:

1.    CASH WILL NOT BE accepted. We will not be responsible for the cash sent or brought to MDA.

2.    Kindly be informed that payment can be combined for a maximum of 5 applications only.

3.    Payment to be made after issuance of payment advice from MDA.

4.    A statement “MDA Regulatory Information Subscription” and Phone No. of the applicant shall be written at the back of the bank draft outside table section.

5.    A receipt of payment will be issued once the bank draft is accepted by the MDA.

6.    Processing time will normally take up to 7 working days after payment is made.

ENQUIRY

Enquiries may be sent to Medical Device Authority (MDA) at the following address:

Medical Device Authority, Ministry of Health Malaysia.

Aras 6, Prima 9, Prima Avenue II,

Block 3547, Persiaran APEC,

63000 Cyberjaya, Selangor.

Email: mdasubscription [AT] mda [DOT] gov [DOT] my

Tel: 03-82300300

Faks: 03-82300200

 

Updated: 31st October 2022

Cetak

Pengumuman

Semua Pengumuman

Suspension and Cancellation of Establishment Licence and Medical Device Registration

Semua establismen yang menjalankan aktiviti meletakkan peranti perubatan dalam pasaran perlu mempunyai Lesen Establismen dan peranti perubatan tersebut perlu didaftarkan seperti yang termaktub dalam Akta Peranti Perubatan 2012 (Akta 737). Orang awam boleh menyemak status Lesen Establismen dan pendaftaran peranti perubatan melalui carian akses di pautan https://mmdr.mda.gov.my/public/

Walau bagaimanapun, terdapat establismen yang telah melanggar Akta 737 dan Peraturan Peranti Perubatan 2012. Read more 

Berita

Semua berita

Safety Information

The following documents are summary of some medical device safety information related to potentially hazardous cases. It only serves as a quick reference and in no way should be considered as exhaustive and up-to-date. Please refer to the source of information and your product supplier for details.

For Listing of Recalls & Listing of Field Safety Notice, please Click Here!

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  Pihak Berkuasa Peranti Perubatan Malaysia,
Kementerian Kesihatan Malaysia,
Aras 6, Prima 9, Prima Avenue II,
Block 3547, Persiaran APEC,
63000 Cyberjaya, Selangor, MALAYSIA

  +603 - 8230 0300
  +603 - 8230 0200 
  mdb [AT] mda [DOT] gov [DOT] my

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  • Kemaskini Terakhir: 29 Mac 2023.
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