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Tissue Level Wide Fixture Digital Lab-Analog

EUDAMEDFDA UDI

Class I (EU MDR)

Ref S-TWFDLA

by Novodent SA

Identity

Trade Name
Tissue Level Wide Fixture Digital Lab-Analog EUDAMED
Implantswiss FDA UDI
Generic Name
Dental implant abutment analog, intraoral-scanning, single-use FDA UDI
Device Name
Bone Level Mini Fixture Lab Analog EUDAMED
Tissue Level Scan Body Implant system for the support of dental prostheses, aimed at restoring missing teeth for aesthetical and functional purposes. Instruments dedicated to implant system for the support of dental prostheses. FDA UDI
Model / Reference
S-TWFDLA EUDAMEDFDA UDI
Description
Tissue Level Scan Body Implant system for the support of dental prostheses, aimed at restoring missing teeth for aesthetical and functional purposes. Instruments dedicated to implant system for the support of dental prostheses. FDA UDI

Identifiers

Catalog Number
S-TWFDLA FDA UDI
Primary DI / UDI-DI
07630188203028 EUDAMEDFDA UDI
Basic UDI-DI
764016818003D7 EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED
GMDN Term
Dental implant abutment analog, intraoral-scanning, single-use 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

Tissue Level Wide Fixture Digital 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 (2)

  • EUDAMED 87c6bd2a-e2c3-463c-b2ba-d4abe6bfe825 61 fields · synced Jul 26, 2026
  • FDA UDI d40b644f-b6d4-405e-910f-3197a60d20ab 35 fields · synced May 30, 2026