Mda.gov.my coupon
Site Title : Official Portal of Medical Device Authority (MDA) Malaysia
Medical Device Authority (MDA) Malaysiahttps://www.mda.gov.my/index.php/announcement/935
Link: https://www.mda.gov.my/index.php/announcement/935-first-edition-guidance-document-mda-gd-0009-rules-of-classification-for-general-medical-devices
FREEWebSECOND EDITION GUIDANCE DOCUMENT MDA/GD/0009: RULES OF CLASSIFICATION FOR GENERAL MEDICAL DEVICES. This Guidance Document was prepared by the Medical Device Authority (MDA) to help the industry and healthcare … ... See DetailsMedical Device Authority (MDA) Malaysiahttps://www.mda.gov.my/index.php/news/794-online
Link: https://www.mda.gov.my/index.php/news/794-online-training-on-good-distribution-practice-for-medical-devices-gdpmd
FREEWebCyberjaya, 15 December 2021 – Medical Device Authority Malaysia (MDA) has organised two days online training on Good Distribution Practice for Medical Devices (GDPMD). … ... See DetailsMedical Device Authority (MDA) Malaysiahttps://portal.mda.gov.my/index.php/doc-list/guidance-document
Link: https://portal.mda.gov.my/index.php/doc-list/guidance-document
FREEWebFeb 2, 2024 · Guidance Documents. These Guidance Document was prepared by the Medical Device Authority (MDA) to help the industry and healthcare professionals in their … ... See DetailsMedical Device Authority (MDA) Malaysiahttps://portal.mda.gov.my/index.php/documents/
Link: https://portal.mda.gov.my/index.php/documents/guidance-documents/1795-requirements-for-labelling-of-medical-devices-1/file
FREEWeb4.8 General contents of labelling. i) An indication of either the batch code/lot number (e.g. on single use disposable medical devices or reagents) or the serial number (e.g. on … ... See DetailsMedical Device Authority (MDA) Malaysiahttps://portal.mda.gov.my/index.php?option=com
Link: https://portal.mda.gov.my/index.php?option=com_content&view=article&id=462&Itemid=515&lang=en
FREEWebHowever, Licensee (s) are required to perform re-certification audit and GDPMD/ISO 13485 certificate must be valid on the expiry date of current licence. Application. Application for … ... See DetailsMedical Device Authority (MDA) Malaysiahttps://mda.gov.my/index.php/ms/dokumen/guidance
Link: https://mda.gov.my/index.php/ms/dokumen/guidance-documents/1857-4-csdt-of-ivd-medical-device-1
FREEWebCopies of certificates or approval letters from each reference agency for the IVD medical device are to be provided as an annex to the CSDT submission. For CE marked devices, … ... See DetailsMalaysia Medical Device Register (MMDR)https://mdar.mda.gov.my/frontend/web/index.php?r
Link: https://mdar.mda.gov.my/frontend/web/index.php?r=carian%2Freport&id=60023
FREEWebfunction turns the device on or off through the infra-red proximity sensor that can detect a hand passed within approximately 10 cm of it. it allows the operator to use the device … ... See DetailsMalaysia Medical Device Register (MMDR)https://mdar.mda.gov.my/frontend/web/index.php?r
Link: https://mdar.mda.gov.my/frontend/web/index.php?r=carian%2Fview&id=12176
FREEWebwondfo one step hiv1/2 whole blood/serum/plasma test (2 lines) is a rapid one step test for the qualitative detection of hiv1/2 antibodies in human whole blood, serum or plasma at … ... See DetailsMedical Device Authority (MDA) Malaysiahttps://portal.mda.gov.my/index.php/documents/
Link: https://portal.mda.gov.my/index.php/documents/guidance-documents/1858-8-csdt-1/file
FREEWebcertificates or reports submitted must be and should be signed-off and dated by the person issuing the report. This person should be authorized to issue such documents. All … ... See DetailsMost Popular Searched
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