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CA Midwest® lmplant 20:1 L

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 1601411-001Model CA&HP

by Bien-Air Dental SA

Identity

Trade Name
CA Midwest® lmplant 20:1 L EUDAMEDFDA UDI
Generic Name
Dental power tool handpiece motorless component FDA UDI
Device Name
CA&HP EUDAMED
Bien-Air Dental contra-angle and straight handpieces are designed to transmit and apply the mechanical energy produced by an electric or air micromotor. FDA UDI
Model / Reference
CA&HP EUDAMED
1601411-001 EUDAMEDFDA UDI
Description
Bien-Air Dental contra-angle and straight handpieces are designed to transmit and apply the mechanical energy produced by an electric or air micromotor. FDA UDI

Identifiers

Primary DI / UDI-DI
J00716014110011 EUDAMEDFDA UDI
Basic UDI-DI
++J007CAHP0001GQ EUDAMED
Direct Marketing DI
J00716014110011 EUDAMED
FDA Product Code
EFB 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
Germany 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 Midwest® lmplant 20:1 L 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 4dd6bb47-f23a-4bb6-adb7-84ff05efa29c 61 fields · synced Oct 5, 2026
  • FDA UDI aa9df343-78c9-45e9-bcf4-e6b230de1bc8 33 fields · synced May 30, 2026