← Back to catalogue

Scanbody

EUDAMEDFDA UDI

Class I (EU MDR)

Ref CAD-SBNBARPModel CAD-SBBBLB0

by Biodenta Swiss AG

Identity

Trade Name
Scanbody EUDAMED
Biodenta FDA UDI
Generic Name
Dental implant abutment analog, intraoral-scanning, single-use FDA UDI
Device Name
CAD-SBBBLB0 EUDAMED
Scan Body with Screw Compatible with Nobel Active RP FDA UDI
Model / Reference
CAD-SBBBLB0 EUDAMED
CAD-SBNBARP EUDAMEDFDA UDI
Description
Scan Body with Screw Compatible with Nobel Active RP FDA UDI

Identifiers

Catalog Number
CAD-SBNBARP FDA UDI
Primary DI / UDI-DI
07640169735523 EUDAMEDFDA UDI
Basic UDI-DI
0764016973CADSBVV EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
Q010207 DENTAL IMPRESSION DEVICES FOR PROSTHETIC DENTISTRY 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
Czechia 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental implant suprastructure, temporary, preformed, single-use

Scanbody by Biodenta Swiss AG — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, temporary, preformed, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Biodenta Swiss AG
EUDAMED SRN
CH-MF-000034374
Authorised Representative
MedNet EC-REP IIb GmbH DE-AR-000011192

Sources (2)

  • EUDAMED b086593d-1f20-49c2-91bd-fe9fef1b16fa 61 fields · synced Jun 18, 2026
  • FDA UDI a878643a-b781-4b50-baa9-015c66c170ea 34 fields · synced May 30, 2026