Albomed GmbH
Germany DE-MF-000007875 Last updated 21 Oct 2026
- Devices
- 261
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
KD Intra-Articular Gel 1.0% Ref 04802
9G-Visc IA 2.2% Ref 04654
KD Intra-Articular Gel 1.6% 2.0 ml Ref 04590
OArt+ 32 1.6% Ref 04304
PRONOLIS HD Mini 1.0% Ref 03472
Synoz Start 1.0% Ref 05311
KD Intra-Articular Gel 2.2% 2.0 ml Ref 00091
OArt+ 120 2.5% Ref 04098
KD Intra-Articular Gel 1.0% 2.0 ml Ref 04739
ArsyVisc 2.2% 2.0 ml Ref 03389
GOaktiv INJEKT ONE 2.5% Ref 05340
KD Intra-Articular Gel 1.0% 2.0 ml Ref 00219
KD Intra-Articular Gel 1.6% 2.0 ml Ref 04713
OArt+ 10 1.0% Ref 04344
GOaktiv INJEKT MINI 1.0% Ref 05336
GOaktiv INJEKT 1.0% Ref 05337
EasyVadin 1.6% 2.0 ml Ref 04960
Synoz Xf 2.2% Ref 05314
OArt+ 44 2.2% Ref 04346
KD Intra-Articular Gel 2.5% 2.0 ml Ref 03968
KD Intra-Articular Gel 2.5% 3.0 ml Ref 05045
EasyVadin 1.6% 1.0 ml Ref 04959
KD Intra-Articular Gel 2.2% 2.0 ml Ref 05044
PRONOLIS HD Mini 1.6% Ref 03426
EasyVadin 1.6% 1.0 ml Ref 04483
9G-Visc IA 1.6% Ref 04652
Synoz Plus 1.6% Ref 05312
EasyVadin 1.6% 2.0 ml Ref 04484
KD Intra-Articular Gel 2.2% Ref 04805
Recosyn uno ultra 2.5% Ref 03468
KD Intra-Articular Gel 2.5% 3.0 ml Ref 05136
KD Intra-Articular Gel 2.2% 2.0 ml Ref 03299
Flexotron Classic 1.0% Ref 03656
Hyalumax 2.2% Ref 04433
Solo 120 2.5% Ref 03413
KD Intra-Articular Gel 1.0% Ref 03277
ArsyVisc 2.5% 4.8 ml Ref 03406
myVISC Bio 1.0% Ref 05445
EasyVadin 1.0% 2.0 ml Ref 04482
KD Intra-Articular Gel 1.0% 1.0 ml Ref 04710
KD Intra-Articular Gel 1.0% 1.0 ml Ref 05145
KD Intra-Articular Gel One 2.5% 3.0 ml Ref 04715
KD Intra-Articular Gel 1.6% 2.0 ml Ref 04804
KD Intra-Articular Gel 1.0% 2.0 ml Ref 04711
KD Intra-Articular Gel 1.6% 2.0 ml Ref 00086
Synoz 1.0% Ref 05453
Flexotron Mini Plus 1.6% Ref 03657
Synsons Xtra 2.2 Ref 00023
Showing 1-50 of 261
EUDAMED certificates
Notified body 0483 3 certificates
- D1478800025 Supplemented
Quality management system EU MDR
- Issued
- 10 Jun 2026
- Expires
- 20 Apr 2031
- Reason
- Other
- D1478800027 Supplemented
Quality management system EU MDR
- Issued
- 24 Jun 2026
- Expires
- 20 Apr 2031
- Reason
- Other
- D1478800026 Supplemented
Technical documentation EU MDR
- Issued
- 10 Jun 2026
- Expires
- 17 Feb 2027
- Reason
- Other
Related companies
Notified bodies
- Notified body 0483
About
ALBOMED GmbH Germany, is one of the leading and most innovative manufacturers for the development and production of viscoelastics – MDR-certified!
Information
- Country
- Germany
- Address
- 11, Hildebrandstraße , Schwarzenbruck, Germany
- Website
- www.albomed.de
- de.linkedin.com/company/albomed
- [email protected]
- Phone
- +49 9183-956982-0
- PRRC contact
- Sven Reese
- EUDAMED SRN
- DE-MF-000007875