Glossary:TAG-00155-Med-Med

Glossary > Medical device

Medical device
Tag-ID	TAG-00155-Med-Med
English	Medical device / Device
EN Abbr.	MD
French	Dispositif médical / Dispositif
FR Abbr.	DM
German	Medizinprodukt / Medizinisches Gerät
DE Abbr.	MP

References

	Scope	Document part	Language	Document
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 3	MD	§ 3	DE	DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 6	MD	§ 6	DE	DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 85	MD	§ 85	DE	DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Annex VIII	MD	Annex VIII	EN	EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 2 Paragraph 1 - 3	MD	Article 2 Paragraph 1 - 3	EN	EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 2 Paragraph 45	MD	Article 2 Paragraph 45	EN	EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 51	MD	Article 51	EN	EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 73	MD	Article 73	EN	EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023
FRA AEC DOC012 v03 Avis aux promoteurs d’investigations cliniques de DM (RIPH1) – Partie II 16-May-2025 3.	MD	3.	FR	FRA AEC DOC012 v03 Avis aux promoteurs d’investigations cliniques de DM (RIPH1) – Partie II 16-May-2025
FRA AEC-DM-DMDIV DOC006 v04 AAP RDM Partie II Modalités pratiques 16-May-2025 -	MD	-	FR	FRA AEC-DM-DMDIV DOC006 v04 AAP RDM Partie II Modalités pratiques 16-May-2025
GBR Directive 93/42/EEC 11-Oct-2007 Article 9	MD	Article 9	EN	GBR Directive 93/42/EEC 11-Oct-2007
GBR MEDDEV 2.7/3 revision 3 May-2015 8	MD	8	EN	GBR MEDDEV 2.7/3 revision 3 May-2015
GBR The Medical Devices Regulations 2002 11-Feb-2021 Article 16 (1) - (3)	MD	Article 16 (1) - (3)	EN	GBR The Medical Devices Regulations 2002 11-Feb-2021
GBR The Medical Devices Regulations 2002 11-Feb-2021 Article 2 medical device	MD	Article 2 medical device	EN	GBR The Medical Devices Regulations 2002 11-Feb-2021
IMDRF IMDRF – Guidelines - -	MD	-	EN	IMDRF IMDRF – Guidelines -
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 3.8	MD	3.8	EN	ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex A - medical device-001	MD	Annex A - medical device	EN	ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex A - medical device-002	MD	Annex A - medical device	EN	ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020
USA 21 CFR Part 50 09-Apr-2025 § 50.3 (j)	G	§ 50.3 (j)	EN	USA 21 CFR Part 50 09-Apr-2025
USA 21 CFR Part 812 09-Apr-2025 § 812.27	MD	§ 812.27	EN	USA 21 CFR Part 812 09-Apr-2025
USA 21 CFR Part 812 09-Apr-2025 § 812.3 (e)	MD	§ 812.3 (e)	EN	USA 21 CFR Part 812 09-Apr-2025
USA 21 CFR Part 812 09-Apr-2025 § 812.3 (f)	MD	§ 812.3 (f)	EN	USA 21 CFR Part 812 09-Apr-2025
USA 21 CFR Part 812 09-Apr-2025 § 812.3 (g)	MD	§ 812.3 (g)	EN	USA 21 CFR Part 812 09-Apr-2025
USA FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023 Sec 510 (k)	G	Sec 510 (k)	EN	USA FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023
USA FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023 Sec 512 (f)	G	Sec 512 (f)	EN	USA FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023
USA FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023 Section 513	MD	Section 513	EN	USA FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023
USA Recognized Consensus Standards - ISO 14155 21-Dec-2020 -	G	-	EN	USA Recognized Consensus Standards - ISO 14155 21-Dec-2020
USA U.S. Code Title 21 30-Sep-2023 § 321 (h)	G	§ 321 (h)	EN	USA U.S. Code Title 21 30-Sep-2023