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Inductive Charger ARCUSdigma III

FDA UDI

Class I (US FDA UDI)

by zebris MEDICAL GmbH

Identity

Trade Name
Inductive Charger ARCUSdigma III FDA UDI
Generic Name
Facebow FDA UDI
Device Name
The inductive charger ARCUSdigma III is an accessory of the facebow ARCUSdigma II and intended for wireless charging of the facebow batteries. FDA UDI
Model / Reference
01570540 FDA UDI
Description
The inductive charger ARCUSdigma III is an accessory of the facebow ARCUSdigma II and intended for wireless charging of the facebow batteries. FDA UDI

Identifiers

Catalog Number
NA FDA UDI
Primary DI / UDI-DI
B915015705401 FDA UDI
FDA Product Code
NFS FDA UDI
GMDN Term
Facebow FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.2060 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Inductive Charger ARCUSdigma III by zebris MEDICAL GmbH — 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
zebris MEDICAL GmbH

Sources (1)

  • FDA UDI b54dc662-48a5-41e9-a71c-a7fba2f3ccec 36 fields · synced May 30, 2026