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Console Chiropro L

FDA UDI

Class I (US FDA UDI)

by Bien-Air Dental SA

Identity

Trade Name
Console Chiropro L FDA UDI
Generic Name
Surgical power tool system control unit, line-powered FDA UDI
Device Name
Chiropro are electrical medical devices used to run dental instruments FDA UDI
Model / Reference
1600613-001 FDA UDI
Description
Chiropro are electrical medical devices used to run dental instruments FDA UDI

Identifiers

Catalog Number
1600613-001 FDA UDI
Primary DI / UDI-DI
J00716006130011 FDA UDI
FDA Product Code
EBW FDA UDI
GMDN Term
Surgical power tool system control unit, line-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4200 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical power tool system control unit, line-powered

Console Chiropro L by Bien-Air Dental SA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical power tool system control unit, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bien-Air Dental SA

Sources (1)

  • FDA UDI 9c92e898-6493-4733-8cb3-73a12c7cb4a8 35 fields · synced May 30, 2026