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Bone Level Multi Unit Abutment Lab Analog

EUDAMEDFDA UDI

Class I (EU MDR)

Ref S-BMUALA40Ref S-BMUALA

by Novodent SA

Identity

Trade Name
Bone Level Multi Unit Abutment Lab Analog EUDAMED
implantswiss FDA UDI
Generic Name
Dental implant suprastructure kit FDA UDI
Device Name
Bone Level Mini Fixture Lab Analog EUDAMED
Bone Level Multi Unit Abutment Lab Analog Implant system for the support of dental prostheses, aimed at restoring missing teeth for aesthetical and functional purposes. Abutment: The part of the system that makes the link between the implant part and the prosthetic super structure. FDA UDI
Model / Reference
S-BMUALA40 EUDAMED
S-BMUALA EUDAMEDFDA UDI
Description
Bone Level Multi Unit Abutment Lab Analog Implant system for the support of dental prostheses, aimed at restoring missing teeth for aesthetical and functional purposes. Abutment: The part of the system that makes the link between the implant part and the prosthetic super structure. FDA UDI

Identifiers

Catalog Number
S-BMUALA FDA UDI
Primary DI / UDI-DI
07630188214352 EUDAMED
07630188201024 EUDAMEDFDA UDI
Basic UDI-DI
764016818003D7 EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED
GMDN Term
Dental implant suprastructure kit FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.3980 FDA UDI
Market of Registration
Türkiye EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Bone Level Multi Unit Abutment Lab Analog by Novodent SA — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

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 (3)

  • EUDAMED 06435778-6546-4920-9b07-227352125f98 61 fields · synced Jul 9, 2026
  • EUDAMED dad96dd7-67bd-4bbf-aac6-94242b4346bb 61 fields · synced May 19, 2026
  • FDA UDI 116498f0-e892-400b-b259-5c45c8779e81 34 fields · synced May 30, 2026