Avinent Implant System Slu
Active in EUDAMEDSpainfrom SRN EUDAMED FDA SRN ES-MF-000013386 FEI 3008791019
- Devices
- 1,358
- Registrations
- EUDAMED·FDA
- FDA recalls
- 0
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Active Regimes: CE MDD Registry: EUDAMED ClassClass:IIb
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Drill Stop DSF6/15 (Guided Surgery) Ref 2795
Active Regimes: CE MDD Registry: EUDAMED ClassClass:IIa- Active Regimes: CE MDD Registry: EUDAMED ClassClass:IIb
- Active Regimes: CE MDD Registry: EUDAMED ClassClass:IIb
RHEIN83® Abutment EC 4.1 GH5 Ref 3279
Active Regimes: CE MDD Registry: EUDAMED ClassClass:IIbDentsply Astra™ Lilac 4.5/5.0 Screw Ref 1895
Active Regimes: CE MDD Registry: EUDAMED ClassClass:IIb- Active Regimes: CE MDD Registry: EUDAMED ClassClass:IIb
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Temporary Abutment CC 4.1 Engaging Ref 3015
Active Regimes: CE MDD Registry: EUDAMED ClassClass:IIb- Active Regimes: CE MDD Registry: EUDAMED ClassClass:IIb
Cemented Abutment EC 3.5 Ø4.5 GH3 Ref 1711
Active Regimes: CE MDD Registry: EUDAMED ClassClass:IIb- Active Regimes: CE MDD Registry: EUDAMED ClassClass:IIb
- Active Regimes: CE MDD Registry: EUDAMED ClassClass:IIb
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- Active Regimes: CE MDD Registry: EUDAMED ClassClass:IIb
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- Active Regimes: CE MDD Registry: EUDAMED ClassClass:IIa
- Active Regimes: CE MDD Registry: EUDAMED ClassClass:IIb
- Active Regimes: CE MDD Registry: EUDAMED ClassClass:IIb
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Drill Stop DSF1/7 (Guided Surgery) Ref 2790
Active Regimes: CE MDD Registry: EUDAMED ClassClass:IIaS&M Premium Kohno TG M Screw Ref 4493
Active Regimes: CE MDD Registry: EUDAMED ClassClass:IIb
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Company details
- EUDAMED SRN
- ES-MF-000013386
- FDA FEI number
- 3008791019
- DUNS number
- 477451012
- EU VAT number
- ESB64286891
- EUDAMED status
- Active
- EUDAMED registered name
- AVINENT IMPLANT SYSTEM S.L.U.
- EUDAMED abbreviated name
- AVINENT
- Registered address
- 107, Carretera de Navarcles, 08251, Santpedor, Spain
- [email protected]
- PRRC contact
- Anna Cortina(public in EUDAMED)
EUDAMED certificates1
1 certificate·1 valid, 0 expired·MDR 1·next expiry 26 Feb 2030
TÜV Rheinland LGA Products GmbH 0197 ·1 certificate
- HZ 1248681-1 Active Supplemented
Quality management system ·EU MDR
- Issued
- 25 Jul 2025
- Expires
- 26 Feb 2030
- Reason
- Other