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Universal Transferbogen System 3D

FDA UDI

Class I (US FDA UDI)

by Ivoclar Vivadent Aktiengesellschaft

Identity

Trade Name
Universal Transferbogen System 3D FDA UDI
Generic Name
Facebow FDA UDI
Device Name
Universal Transfer Bow System 3D FDA UDI
Model / Reference
593710 FDA UDI
Description
Universal Transfer Bow System 3D FDA UDI

Identifiers

Catalog Number
593710 FDA UDI
Primary DI / UDI-DI
DIVO5937101 FDA UDI
FDA Product Code
KCR FDA UDI
GMDN Term
Facebow FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3220 FDA UDI
Commercial Distribution
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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Facebow

Universal Transferbogen System 3D by Ivoclar Vivadent Aktiengesellschaft — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Facebow.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ivoclar Vivadent Aktiengesellschaft

Sources (1)

  • FDA UDI c73f72c5-3521-443e-afe4-88a3c779ac15 34 fields · synced Jun 8, 2026