MDD Distributor Registration Requirements

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Q MDD - distributor EU Medical Device Regulations 1
K Obligation for Distributor in MDD/MDR CE Marking (Conformité Européene) / CB Scheme 4
Q Class I Medical Device with measuring function (UK MDR 2002 / MDD) UK Medical Device Regulations 3
K MDD to MDR Other Medical Device and Orthopedic Related Topics 1
K Subcontractors Providing Services Under MDD or MDR need ISO 13485 from EU Notified Body? CE Marking (Conformité Européene) / CB Scheme 5
K Selling legacy device under MDD to India EU Medical Device Regulations 1
G Updating MDD devices after MDR transitional period EU Medical Device Regulations 0
P Servicing of Class IIb devices under MDD EU Medical Device Regulations 2
G Significant changes on MDD devices/Old Devices after MDR transitional period EU Medical Device Regulations 1
S Changing PCB Assembler and impact on QMS and MDD CE Certificate EU Medical Device Regulations 2
Ed Panek Auditor Comment about MDR vs MDD EU Medical Device Regulations 10
O MDD 93/42 and making documentation available EU Medical Device Regulations 1
M Reworking MDD product w MDR labeling CE Marking (Conformité Européene) / CB Scheme 5
A Declaring Conformity with MDR Article 120(3) for an MDD Legacy Device EU Medical Device Regulations 1
L Significant subcontractor update, still under MDD Certification, possible? CE Marking (Conformité Européene) / CB Scheme 3
M MD Class I transition period MDD to MDR - changes? EU Medical Device Regulations 1
marmotte MDD legacy until 2024 - EUDAMED, role (and cost!) of the EC Rep EU Medical Device Regulations 6
H MDD VS MDR 2002-218 UK Medical Device Regulations 6
S MDD to MDR - Tallow Derivatives Impact EU Medical Device Regulations 1
M Post Market Safety Update Report for devices that will be up-classified under MDR but are currently under MDD EU Medical Device Regulations 6
Fjalar Spare parts for discontinued MDD compliant class I medical device EU Medical Device Regulations 4
chris1price Notified Body responsible for product safety under MDD? EU Medical Device Regulations 4
Ed Panek Upcoming NB MDD ---> MDR Crunch EU Medical Device Regulations 0
JoCam Rental and MDD versus MDR EU Medical Device Regulations 1
Ed Panek Notified Body Substantial Change MDD EU Medical Device Regulations 1
J How to keep MDD certificate valid when legal manufacturer has liquidity problem EU Medical Device Regulations 0
Ed Panek MDD Cleared Private Labelled Devices into EU EU Medical Device Regulations 0
K Section 13.6 Annex 1 MDD 93/42/EEC for Glove EU Medical Device Regulations 0
Ed Panek IFU Contact Requirements - FDA and MDD/MDR US Food and Drug Administration (FDA) 1
U MDD Article 12/ MDr Article 22 interpretation EU Medical Device Regulations 2
E Our company is planning to file MDD not MDR next month. Do we require to show chemical characterization report ? CE Marking (Conformité Européene) / CB Scheme 2
S Converting SOP MDD to MDR Noob ISO 13485:2016 - Medical Device Quality Management Systems 4
silentmonkey Are risks in supply chain and development activities within scope of MDD? EU Medical Device Regulations 4
A First CE-mark class III implantable device under MDD EU Medical Device Regulations 8
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 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
R Applicability of new non-harmonized standards (MDD/MDR) EU Medical Device Regulations 14
N Label Placement Requirement in MDD/MDR EU Medical Device Regulations 3
K Measuring Function MEDDEV 2.1/5 relation with MDD 93/42/EEC CE Marking (Conformité Européene) / CB Scheme 2
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

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