Medical Devices technical lists for Germany, Austria, Sweden, Switzerland, etc.

D

Danteh

#1
Hi! In my company we are currently developing a new area of expertise related to Medical Devices (MD) reimbursement.

I?m looking for a technical list of medical devices (used in a hospital setting) in many different countries, but it seems like it?s not publicly available.

For example, for Switzerland I have found the MiGeL/LiMA list, but from what I?ve seen it describes mainly medical devices used in a non-hospital setting. I?m especially interested in MDs for the cardiology therapeutic area (pacemakers, coronary stents, etc) with technical specifications of the device, manufacturers, national code, tariffs, etc.

From what I've found some countries have very comprehensive MD databases (Australia, for example: I can't post links but if you go to: search-au.funnelback.com/s/search.html?query=heart+valve&collection=tga-artg you'll find it); but I can't seem to find anything similar for the aforementioned countries.

Any guidance regarding this matter would be greatly appreciated.

:thanx:
 
Elsmar Forum Sponsor

Stijloor

Leader
Super Moderator
#2
A Quick Bump!

Can someone help?

If you had your questions answered in the Cove Forums, please consider helping others.

Thank you very much!
 
Thread starter Similar threads Forum Replies Date
M Informational USFDA draft guidance – Technical Considerations for Non- Clinical Assessment of Medical Devices containing Nitinol Medical Device and FDA Regulations and Standards News 0
M Medical Devices and ASD-STE100 (Simplified Technical English) Other Medical Device Related Standards 0
shimonv CFDA Technical Guidelines for Clinical Evaluation on Medical Devices (English) China Medical Device Regulations 8
M Technical File Locations - Class I and Class IIa Medical Devices EU Medical Device Regulations 3
S Technical File Submission? - Medical Devices no longer made EU Medical Device Regulations 10
S Technical File Review to updated MDD 93/42/EC (Class II medical devices) EU Medical Device Regulations 3
J Technical File vs. Design Dossier - Class II and Class III Medical Devices ISO 13485:2016 - Medical Device Quality Management Systems 12
R Assessment of Technical Information of Annex II Medical Devices ISO 13485:2016 - Medical Device Quality Management Systems 2
M MDSAP Medical Devices Suppliers Canada Medical Device Regulations 5
C. Tejeda Process validation of rework assembly methods (medical devices) Medical Device and FDA Regulations and Standards News 2
N FDA medical devices US Food and Drug Administration (FDA) 1
BusyBee GIVD codes for In-vitro medical devices EU Medical Device Regulations 2
J0anne How to find Certifying Bodies for US based & sold Medical Devices? US Medical Device Regulations 11
Newbie22 UPDATE UKCA; UK 12 month extension (Future regulation of medical devices - extension of standstil period) UK Medical Device Regulations 4
S Local (country) registration of medical devices - Who does it in best case? Other Medical Device Regulations World-Wide 2
G Labeling requirements for REFURBISHED medical devices EU Medical Device Regulations 0
L Selling medical devices from USA in EU markets CE Marking (Conformité Européene) / CB Scheme 1
H Active Implantable Medical Devices - ISO 14708 and EN 45502 Other Medical Device Related Standards 0
P Requirements for Exporting Medical Devices to Libya Other Medical Device Regulations World-Wide 2
T Peru Veterinary Medical Devices Other Medical Device Regulations World-Wide 0
H Medical Devices Regulatory Intelligence for International Markets ISO 13485:2016 - Medical Device Quality Management Systems 1
V Retrospective validation medical devices Qualification and Validation (including 21 CFR Part 11) 7
K 2021/2226 on Electronic Instructions for Use (IFU) for medical devices Article 22 Packs EU Medical Device Regulations 1
C Is there a definition of accessories for medical devices in China? China Medical Device Regulations 1
A Registration of medical devices in Greece EU Medical Device Regulations 5
I Customer Feedback Medical Devices ISO 13485:2016 - Medical Device Quality Management Systems 6
L Non Applicability of Clauses in ISO13485 for Medical Devices Medical Device and FDA Regulations and Standards News 4
M Medical Devices - DFM Medical Device and FDA Regulations and Standards News 5
B Transport Validation For Non-sterile Medical Devices ISO 13485:2016 - Medical Device Quality Management Systems 4
S Post Market Surveillance Report (PMSR) for Medical Devices EU Medical Device Regulations 6
A Mandatory Languages Requirements for Medical Devices CE Marking (Conformité Européene) / CB Scheme 2
N Shelf life guidance EU MDR, class 1 and class 2 Medical Devices EU Medical Device Regulations 2
B Do I need a Cleanroom to manufacture Medical Devices? ISO 13485:2016 - Medical Device Quality Management Systems 2
Derrick Yang 各国医疗器械上市流程的区别 (Differences in the listing process of medical devices in various countries) Service Industry Specific Topics 3
Judy Abbott Guideline as for devices utilizing plants and their derivatives in medical device US Food and Drug Administration (FDA) 6
Q Finding Independent License Holder (Medical devices) in Philippines Other Medical Device Regulations World-Wide 1
M Custom made class 1 Medical devices EU Medical Device Regulations 3
G Need Help with Run @ Rate for Medical Devices ISO 13485:2016 - Medical Device Quality Management Systems 0
S ISO 14644 Cleanrooms: Industry-Specific Requirements for Medical Devices Other Medical Device Related Standards 0
I Post-market surveillance and Post-market performance follow-up for in vitro diagnostic medical devices EU Medical Device Regulations 0
JoCam Accessories for medical devices EU Medical Device Regulations 5
M Prescription Form - Medical Devices US Food and Drug Administration (FDA) 2
XRAY_3121 Drop Shipping Legend Medical Devices Other Medical Device Related Standards 0
A Production line for medical devices Other Medical Device Related Standards 1
S Design & Development records for Medical Devices Packaging and Labelling ISO 13485:2016 - Medical Device Quality Management Systems 9
K MHLW MO169 2021 Japan Ministerial Ordinance on Standards for Manufacturing Control and Quality Control for Medical Devices and In-Vitro Diagnostics Japan Medical Device Regulations 2
U Medical Devices Labeling Medical Device and FDA Regulations and Standards News 0
K Guidance on X-Ray Medical Devices for Animal Use - FDA US Food and Drug Administration (FDA) 0
dgrainger Informational Good news: Commission proposes a progressive roll-out of the new In Vitro Diagnostic Medical Devices Regulation EU Medical Device Regulations 3
dgrainger Informational MDCG 2021-24 - Guidance on classification of medical devices EU Medical Device Regulations 0

Similar threads

Top Bottom