← Back to catalogue

Implantswiss

FDA UDI

Class I (US FDA UDI)

by Novodent SA

Identity

Trade Name
Implantswiss FDA UDI
Generic Name
Dental implant suprastructure kit FDA UDI
Device Name
Bone Level Impression Coping Transfer Non-Hex Long "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-BICTN55L FDA UDI
Description
Bone Level Impression Coping Transfer Non-Hex Long "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-BICTN55L FDA UDI
Primary DI / UDI-DI
07640168183080 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant suprastructure kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Implantswiss by Novodent SA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Novodent SA

Sources (1)

  • FDA UDI 575d51a9-ef52-4c65-aef6-552b1cab08e9 36 fields · synced Jun 8, 2026