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Mesyuarat ASEAN Medical Device Technical…

6 - 7 Mac 2024 - Mesyuarat ASEAN Medical Device Technical Committee (AMDTC) kali ke-13...

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FUTURE HEALTHCARE ASIA 2024

6 & 7 Mac 2024 – Baru-baru ini telah berlangsung program “Future Healthcare Asia 2024”...

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MDA, Malaysia dan MFDS, Korea Selatan Me…

26 Februari 2024 – Pihak Berkuasa Peranti Perubatan Malaysia (MDA), Malaysia dan 'Ministry of Food...

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LAWATAN KERJA TURKIYE MEDICAL INDUSTRY C…

Cyberjaya, 27 Februari 2024 - Turkiye Medical Industry Cluster Association (OSTİM), yang mewakili 120 syarikat...

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Media Coverage (Newspaper Cutting)

2024 Majlis Soft Launch Asia’s International Medical Technology Exhibition And Conference (ASIAN MEDTEC 2024) Dan Bersempena...

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BENGKEL KOMPETENSI BIOMEDICAL TECHNICAL …

Bertempat di Pejabat Pihak Berkuasa Peranti Perubatan pada 14-15 Februari 2024, telah berlangsungnya Bengkel Kompetensi...

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PROGRAM PENGUKUHAN INTEGRITI: “AMANAH:JA…

CYBERJAYA, 16 Feb - Program Pengukuhan Integriti bertajuk “Amanah:Jangan Sampai Punah” telah diadakan pada Jumaat...

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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.

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KENALI BENTUK SUAPAN (RASUAH)

29-12-2023

  Dikemaskini: 29 Disember 2023

LARANGAN MENJALINKAN HUBUNGAN SULIT / SKANDAL

29-12-2023

  Dikemaskini: 29 Disember 2023

MDA TEMPAT KERJA BEBAS DADAH (TEKAD)

29-12-2023

  Dikemaskini: 29 Disember 2023 

WAKTU BEKERJA FLEKSI

29-12-2023

  Dikemaskini: 29 Disember 2023

TATAKELAKUAN PENJAWAT AWAM

29-12-2023

  Dikemaskini: 29 Disember 2023

PEMAKAIAN PAKAIAN BATIK MALAYSIA SEMASA WAKTU BEKERJA…

29-12-2023

  Dikemaskini: 29 Disember 2023

LARANGAN STAF PIHAK BERKUASA PERANTI PERUBATAN TERLIBAT…

29-12-2023

  Dikemaskini: 29 Disember 2023

PERISYTIHARAN HARTA DAN LIABILITI

29-12-2023

  Dikemaskini: 29 Disember 2023

LARANGAN PENERIMAAN DAN PEMBERIAN HADIAH YANG BERKAITAN…

29-12-2023

  Dikemaskini: 29 Disember 2023

AKTA BADAN-BADAN BERKANUN (TATATERTIB DAN SURCAJ) 2000…

29-12-2023

  Dikemaskini: 29 Disember 2023

KETERHUTANGAN KEWANGAN YANG SERIUS

29-12-2023

  Dikemaskini: 29 Disember 2023

POSSIBLE WAYS TO REGISTER IVD ANALYZER

16-11-2023

        Updated: 16 November 2023 

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

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Medical Device Authority (MDA),
Ministry of Health Malaysia,
Level 6, Prima 9, Prima Avenue II,
Block 3547, Persiaran APEC,
63000 Cyberjaya, Selangor, MALAYSIA

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