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Ca 20:1

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 1600632-001Model CA&HP

by Bien-Air Dental SA

Identity

Trade Name
CA 20:1 EUDAMEDFDA UDI
Generic Name
Dental power tool handpiece motorless component FDA UDI
Device Name
CA&HP EUDAMED
CA and HP are intended to transmit and apply the mechanical energy produced by a dental air or electric micromotor. They contain the gearing necessary for maintaining, increasing or reducing the micromotor's speed FDA UDI
Model / Reference
CA&HP EUDAMED
1600632-001 EUDAMEDFDA UDI
Description
CA and HP are intended to transmit and apply the mechanical energy produced by a dental air or electric micromotor. They contain the gearing necessary for maintaining, increasing or reducing the micromotor's speed FDA UDI

Identifiers

Catalog Number
1600632-001 FDA UDI
Primary DI / UDI-DI
J00716006320011 EUDAMEDFDA UDI
Basic UDI-DI
++J007CAHP0001GQ EUDAMED
Direct Marketing DI
J00716006320011 EUDAMED
FDA Product Code
EBW FDA UDI
EMDN Code
Z12110199 INSTRUMENTS FOR DENTAL TREATMENT UNITS - OTHER EUDAMED
GMDN Term
Dental power tool handpiece motorless component FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
872.4200 FDA UDI
Market of Registration
Austria EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Ca 20:1 by Bien-Air Dental SA — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bien-Air Dental SA
EUDAMED SRN
CH-MF-000014661
Authorised Representative
Bien-Air Europe Sàrl FR-AR-000011942

Sources (2)

  • EUDAMED 52620421-36b0-4f1d-8b47-87bcff2d44af 61 fields · synced Aug 2, 2026
  • FDA UDI 9523397a-44be-4a2c-9bcc-f0e38faf0468 35 fields · synced May 30, 2026