Factsheet for Class I – Medical Devices | 28 April 2021
European commission published a Factsheet for Class I- Medical Devices based on MDCG 2019-5 rev. 1.
for class I medical device manufacturers. It summarizes the necessary steps to ensure the compliance of
class I medical with applicable requirements of the EU-MDR 2017/745. The class I medical devices includes
devices which are already placed in the market under MDD requirements and new devices expected to place
on the market. The FAQ give in factsheet helps to understand the requirements for Instruction for use and
labels for class I device.
Guidance on basic UDI-DI and changes to UDI-DI MDCG 2018-1 Rev.4 | 27 April 2021
Medical Device Coordination Group issued a Guidance on BASIC UDI-DI and changes to UDI-DI. This
guidance explains the Basic UDI-DI & explain requirements of new UDI-DI for the device. The Basic UDIDI is the primary key. It is not visible on any trade item. Basic UDI-DI is used for connecting devices with
same intended purpose, risk class and essential design and manufacturing characteristics.
The new UDI-DI should be assigned to the device whenever there is a change that will lead to mislead the
traceability of the device. These include changes in the following:
• Name or trade name
• Device version or model
• Labelled as single use
• Packaged sterile
• Need for sterilization before use
• Quantity of devices provided in a package
• Critical warnings or contra-indications (e.g. Containing latex or dehp)
• CMR /endocrine disruptors.
Regulation (EU) 2017/745 – Questions & Answers regarding clinical investigation MDCG
2021-6 | 22 April 2021
Medical Device Coordination Group published Regulation (EU) 2017/745 – Questions & Answers regarding
clinical investigation. This document is intended for clinical investigation sponsors. The Q&A lays out the
regulatory pathway for clinical investigations, also delivers guidance on difference between requirements
as per EU-MDR compared to Directive 93/42/EEC and 90/385/EEC, pilot clinical investigation, responsibilities of sponsor, safety reporting requirements, modifications to clinical investigations, timeline for clinical investigations, clinical investigation reports, arrangement for the transitional period.
Guidance on standardization for medical devices MDCG 2021-5 | 16 April 2021
Guidance on standardization for medical devices by MDCG explains general framework, development, and standardization of different harmonized European standards in support of the new legislative framework if the EU for medical device. The new EU legislative framework on medical devices consists of three current Directives and two new Regulations. The guidance also provides adequate reference list for legal and guidance framework of EU.
Commission implementing decision (EU) 2021/611 | 14 April 2021
Following standards have been included in list of harmonized standards on biological evaluation of medical
devices, packaging for terminally sterilized medical devices, sterilization of health care products and
clinical investigation of medical devices for human subjects:
EN ISO 10993-16:2017
EN ISO 10993-18:2020
EN ISO 11607-1:2020
EN ISO 11737-2:2020
EN ISO 14155:2020
EN ISO 11607-2:2020
Application of transitional provisions for certification of class D in vitro diagnostic medical devices according to Regulation (EU) 2017/746 MDCG 2021-4 | 09 April 2021
This document by Medical device coordination group includes indications for IVDR provisions for class D device related to notified body and EU reference laboratory (EURL) during transition period of EU legislation till 26 May 2022. According to EU IVDR, in vitro medical device manufacturer needs to submit
an application to notified body. As a part of conformity assessment for class D devices, whenever necessary specific elements might be reviewed by experts panel or tested in EURL. This guidance issue helps class D IVD manufacturer.
Updated Implementation Rolling Plan – Regulation (EU) 2017/745 and Regulation (EU) 2017/746 | 09 April 2021
The implementation rolling plan list down essential implementing acts and other relevant initiatives that the European commission has approved or will do so in the future.
Medicines and Medical Devices Act 2021
An Act has been passed by UK government for patient safety related to human medicines and medical devices, veterinary medicines. This bill is to ensure the human safety by providing the regulations, enforcements for manufacture, marketing, and sales.
MHRA fees | 1 April 2021
The UK Government has published a new guidance to understand the changes to MHRA fees for 2021 – This guidance includes current MHRA fees for different categories of license, fees definition. These fees have come in force from 1 January 2021.
FDA Emergency Use Authorization (EUA) routes for medical devices: Updated overview
April 5 2021
Due to Covid-19 last year FDA issued Emergency Use Authorization route for the in vitro diagnostics for the detection and/or diagnosis of COVID-19 personal respiratory protective devices, and other medical devices, including alternative products used as medical devices. This list has been updated with new tests and devices.
ASCA-Accredited Testing Laboratories | 14 April 2021
The FDA announces medical device testing laboratories accredited under ASCA program.
Medical Device Classification Regulations to Conform to Medical Software Provisions in the 21st Century Cures | 19 April 2021
FDA removes some software functions from medical device classification regulations to reflect the changes to the Federal Food, Drug, and Cosmetic Act (FD&C Act) made by the 21st Century Cures Act (the Cures Act). This rule updates eight classification regulations. They do not include software functions that are excluded from the device definition by section 520(o)(1) of the FD&C Act hence does not fall under FDA’s device statutory authority.
Notice: Technical requirements for anti-microbial claims for medical masks | 21 April 2021
Health Canada publishes the notice for safety and effectiveness requirements for class I medical masks and face coverings with antimicrobial claims. Face covers protecting the face from droplets or air particle without the anti-microbial claims are not considered as medical device. All new class I medical device mask with claim should support evidence and reports of necessary test for example Bacterial Filtration Efficiency (BFE). Notice lists down total of nine safety and effectiveness requirement.
Digitization of package inserts | 27 April 2020
Japan PMDA issues guidance on package insert digitization requirements. Due to Pharmaceutical Machinery Act from now all the package inserts will be replaced by GS1 barcode or two-dimensional code which will contain the information regarding medical device. This code will be scanned by PI (Package
insert)-navi, A Smartphone App on phone or tablet to read the information like Emergency safety information such as package inserts, revision instruction reflection history, examination report / re-examination report, etc.
Regulation of CT Scan equipment, All Implantable Devices, MRI equipment etc. as Drugs with effect from April 1st 2021
CDSCO India has passed an order for all implantable devices, CT scan equipment, MRI equipment, Defibrillators, PET equipment Dialysis machine, X-ray machine and bone marrow cell separator. According to the order importers and manufacturers are required to take import/manufacturing license from the
central licensing authority or state licensing authority from 1st April 2021 onwards.
TGA presentation: The regulation of medical device software | 14 April 2021
Therapeutic goods administration (TGA) of Australia has published the presentation on the regulation of medical device software on their website. The presentation gives information on when a software can be considered as a medical devices and regulatory changes for medical device software.
NMPA publishes guidelines for Device Master File (DMF) submissions | April 2021
National Medical Products Administration (NMPA) has released the guidance for DMF record filing requirements. It includes the necessary registration data for DMF filing application process for filing or renewal of DMF. CMDE has announced the electronic DMF submissions using eRPS system. This announcement has included the guidance for application to become Certificate authority and format and content of DMF.
NMPA China Allows Laboratory Developed Test (LDT) | 29 April 2021
The new “Regulation for Medical Device Administration and Supervision”, Order 739 effecting from 1st June 2021 is replacing the Order 680. Article 53 in the order 739 allows the development of laboratory developed test (LDT) in China. It allows the china medical institution to develop its own IVD reagents based on the clinical needs of the institutions. The medical institutions should meet certain criteria to produce its own IVD reagents.
Class II Medical Device Guidelines March 2021 | 16 April 2020
NMPA’s Center of Medical Device Evaluation (CMDE) and local testing centers has published the Class II medical device guidelines for 22 medical devices. This guideline instructs the renewals and new registrations process for the 22 Class II medical devices. Guidelines for devices used in Clinical Chemistry,
Orthopedic, General Hospital, Anesthesiology, Radiography, Gastroenterology / Urology has been issued.
Deployment of Pakistan Integrated Regulatory Information Management System At DRAP| 26 April 2020
Drug regulatory authority of Pakistan (DRAP) commences the use of Pakistan Integrated Regulatory Information Management System (PIRIMS) for the optimization of regulatory submission process. This digital platform will be used for new online applications of new drug manufacturing licenses (DML). The direct submission for DML will not be accepted.
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