Implants Diffusion International
Active in EUDAMEDFrancefrom SRN EUDAMED SRN FR-MF-000000597
- Devices
- 313
- Registrations
- EUDAMED
Catalogue
1014 Ref 1014
2335 Ref 2335
2220P Ref 2220P
2340N Ref 2340N
M114 Ref M114
322l Ref 322L
G10J Ref G10J
0146 Ref 0146
G9B Ref G9B
C146 Ref C146
2520P Ref 2520P
Sbht Ref SBHT
1242TD Ref 1242TD
R1230 Ref R1230
322E Ref 322E
AL63 Ref AL63
RL63 Ref RL63
2004NL Ref 2004NL
Pih Ref PIH
C1228 Ref C1228
X1238 Ref X1238
Trousse IDPRO Ref Trousse IDPRO
815 Ref 815
2320P Ref 2320P
EX12M Ref EX12M
X1242TD Ref X1242TD
C1252 Ref C1252
73CL Ref 73CL
0931 Ref 0931
Trousse IDSlim Ref Trousse IDSlim
820N Ref 820N
0122 Ref 0122
D4 Ref D4
154223 Ref 154223
905 Ref 905
0246 Ref 0246
409 Ref 409
Trousse IDAll TD Ref Trousse IDAll TD
Trousse ID3 Ref Trousse ID3
0116 Ref 0116
G7V Ref G7V
1036 Ref 1036
RL43 Ref RL43
433 Ref 433
R835 Ref R835
124223 Ref 124223
1520 Ref 1520
F04 Ref F04
G1535 Ref G1535
423A Ref 423A
Showing 151-200 of 313
Company details
- EUDAMED SRN
- FR-MF-000000597
- SRN (system / procedure pack)
- FR-PR-000050293
- EU VAT number
- FR54343586236
- EUDAMED status
- Active
- EUDAMED registered name
- Implants Diffusion International
- EUDAMED abbreviated name
- IDI
- Registered address
- 23-25, Rue Emile Zola, 93100, Montreuil, France
- Website
- www.idi-dental.com/
- [email protected]
- Phone
- +33149707048
- PRRC contact
- Berentha THAMBOO
EUDAMED certificates
1 certificate1 valid, 0 expiredMDR 1next expiry 12 May 2030
Notified body 1639 1 certificate
- FR25/00000112 Issued
Quality management system EU MDR
- Issued
- 12 May 2025
- Expires
- 12 May 2030
From the company website
IDI – Implants Diffusion International, French designer and manufacturer of implants dental since 1987. Label Origin France Warranty, CE marking EU-MDR 2017/745.
What Implants Diffusion International makes
Implants Diffusion International manufactures dental, prosthetic, and surgical drills, including models designed for precision cutting and tissue preparation in clinical settings. Their product line covers a range of applications, from dental implantology to orthopedic and maxillofacial procedures, with devices tailored for both manual and powered use.
The company’s devices are classified under EU Medical Device Regulations as Class I, Class II, and Class IIa, with listings in the EUDAMED database and FDA’s 510(k) clearance registry. The manufacturer is based in France, adhering to regulatory requirements for medical devices in both European and U.S. markets.