MDD Harmonized List of Standards Website Moved

Marc

Hunkered Down for the Duration
Staff member
Admin
#1
On 2 Feb 2015 the previous site for the List of Harmonized Standards for the MDD and other Medical Device Directives (AIMDD & IVDD) moved to a new location.

The old MDD Harmonized Standards Listing used to be located at the website address of http://ec.europa.eu/enterprise/poli...onised-standards/medical-devices/index_en.htm but as of 2 Feb 2015 the site has been archived. The new site can be found by following the instructions on the archived site.
 
Elsmar Forum Sponsor

Ronen E

Problem Solver
Staff member
Moderator
#2
It's not just the harmonized standards pages, it's the whole Europa / Enterprise website.

They did a facelift(?) but also chopped some organs on the way... :(

Good thing that all the old pages are still accessible online (with an "Archived 2.2.2015" label), though I don't know for how long.
 
Thread starter Similar threads Forum Replies Date
G Harmonized List - MDD 93/42/EEC Other ISO and International Standards and European Regulations 2
W New list of MDD Harmonized Standards Other Medical Device Related Standards 2
xcanals_tecno-med.es Revised List of Harmonized Standards for Medical Device Directives (MDD) in the EU EU Medical Device Regulations 48
W New List of Medical Device Harmonized Standards - MDD CE Marking (Conformité Européene) / CB Scheme 5
A List of Harmonized Standards for the MDD, IVD and IMDD - June 2006 ISO 13485:2016 - Medical Device Quality Management Systems 5
R Applicability of new non-harmonized standards (MDD/MDR) EU Medical Device Regulations 8
W New Harmonized Standards MDD and IVDD EU Medical Device Regulations 5
Y CE Mark & Harmonized Standards - Article 5.1, MDD - Has anyone challanged this? EU Medical Device Regulations 5
W EN ISO 13485:2003 harmonized to AIMD, MDD and IVDD ISO 13485:2016 - Medical Device Quality Management Systems 2
S Are risks in supply chain and development activities within scope of MDD? EU Medical Device Regulations 3
A First CE-mark class III implantable device under MDD EU Medical Device Regulations 8
Q MDD - distributor EU Medical Device Regulations 1
R MDD x PPE Directive - Statement of Non-Applicability EU Medical Device Regulations 3
D Does Manufacture can submit CE mark application under MDD with NB for his New product after May 2020? EU Medical Device Regulations 3
H MDD Article 12 Labeling for Class IIa Medical Device - Please Advise EU Medical Device Regulations 3
M Requirements for an MDD approved device after 26/05/2021 EU Medical Device Regulations 3
H MDD CM, MDR manufacturer. 2020. Is it ok? EU Medical Device Regulations 1
S Technical File for Surgical Mask in Class 1 MDD Elsmar Cove Forum ToS and Forum Policies 1
S MDR Delay - MDD design Change? (before new MDR DOA) EU Medical Device Regulations 8
P What ASTM std is EC 93/42 MDD EQUIVALENT TO CE Marking (Conformité Européene) / CB Scheme 1
N Label Placement Requirement in MDD/MDR EU Medical Device Regulations 1
Kuldeep Singh Measuring Function MEDDEV 2.1/5 relation with MDD 93/42/EEC CE Marking (Conformité Européene) / CB Scheme 1
A Class medical device (MDD) - Classification help EU Medical Device Regulations 1
Z Economic Operators Responsibilities after DOA for legacy MDD devices EU Medical Device Regulations 2
J MDD to MDR transition - Time required for the implementation of the MDR EU Medical Device Regulations 7
F MDR system/procedurepack (article 22) with device acc. to MDD and MDR CE Marking (Conformité Européene) / CB Scheme 2
I Maintaining Technical Documentation under MDD and MDR EU Medical Device Regulations 1
P Adding "new" medical device to existing CER - under MDD CE Marking (Conformité Européene) / CB Scheme 1
Watchcat Duration of MDD Certification EU Medical Device Regulations 4
Z MDD ER 7.5, "phthalate test"? Aspiration tips EU Medical Device Regulations 3
R Notified Body for MDD 1Q20 - Florida Company Registrars and Notified Bodies 4
S Until when can we CE-mark and sell MDD class 1 devices? CE Marking (Conformité Européene) / CB Scheme 17
D CE Marking Requirements MDD & MDR - new product development covered under same scope EU Medical Device Regulations 1
B Accredited laboratory or not under MDD 93/42/EEC IEC 60601 - Medical Electrical Equipment Safety Standards Series 11
T Custom made medical device MDD vs MDR definition CE Marking (Conformité Européene) / CB Scheme 12
Watchcat MDD, MDR/IVDR, Working Groups, Expert Panels, MEDDEVs and Other EU Guidances EU Medical Device Regulations 32
D MDD Certification Validity after May 2020 EU Medical Device Regulations 12
A Compatibility between MDD and MDR devices EU Medical Device Regulations 7
M Device CE certified under MDD / MDR > new GTIN? EU Medical Device Regulations 7
N When is "placing on the market"? MDD certified medical devices EU Medical Device Regulations 32
G Essential Requirements Checklist - (MDD 93/42 / EEC) Misc. Quality Assurance and Business Systems Related Topics 2
K EU MDD Class I Device market access / certification after 26th May 2020 EU Medical Device Regulations 9
V CE Mark under MDD or IVDR - IVD company doing Virtual Manufacturing Other Medical Device Regulations World-Wide 3
JoshuaFroud The withdrawal of Lloyd’s Register MDD & IVDD Notified Body Status CE Marking (Conformité Européene) / CB Scheme 1
A How to manage the QMS system and SOP during the transition from MDD to MDR EU Medical Device Regulations 4
F Class I Device under MDD, reclassified to Class II under MDR Other Medical Device Related Standards 5
S Dual MDD and MDR certification EU Medical Device Regulations 7
Kuldeep Singh Obligation for Distributor in MDD/MDR CE Marking (Conformité Européene) / CB Scheme 4
D MDD to MDR - Technical File conversion EU Medical Device Regulations 4
shimonv Checklist for MDD to MDR gap analysis EU Medical Device Regulations 17

Similar threads

Top Bottom