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Bone Level Fixture Hybrid

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref S-BFHR4314

by Novodent SA

Identity

Trade Name
Bone Level Fixture Hybrid EUDAMED
Implantswiss FDA UDI
Generic Name
Screw endosteal dental implant, two-piece FDA UDI
Device Name
Bone Level Fixture Hybrid EUDAMED
Bone level Fixture Hybrid SRA 4.3 x 14 mm Implant system for the support of dental prostheses, aimed at restoring missing teeth for aesthetical and functional purposes. Implant: The part of the system that is inserted in and connected to the jaw bone to allow for prosthesis superstructure fixation, which includes an abutment. FDA UDI
Model / Reference
S-BFHR4314 EUDAMEDFDA UDI
Description
Bone level Fixture Hybrid SRA 4.3 x 14 mm Implant system for the support of dental prostheses, aimed at restoring missing teeth for aesthetical and functional purposes. Implant: The part of the system that is inserted in and connected to the jaw bone to allow for prosthesis superstructure fixation, which includes an abutment. FDA UDI

Identifiers

Catalog Number
S-BFHR4314 FDA UDI
Primary DI / UDI-DI
07640168180126 EUDAMEDFDA UDI
Basic UDI-DI
B-07640168180126 EUDAMED
510(k) Number
K181266 FDA UDI
FDA Product Code
DZE FDA UDI
EMDN Code
P01020101 DENTAL IMPLANTS EUDAMED
GMDN Term
Screw endosteal dental implant, two-piece FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
872.3640 FDA UDI
Market of Registration
Sweden EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Bone Level Fixture Hybrid by Novodent SA — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Novodent SA
EUDAMED SRN
CH-MF-000023309
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED c53feff0-6acb-41a8-be95-68d08d943a24 61 fields · synced Jun 19, 2026
  • FDA UDI 7c196a48-129a-49f1-a6f9-17244d121a59 36 fields · synced May 30, 2026