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Coupling Multiflex 4h L

FDA UDI

Class I (US FDA UDI)

by Bien-Air Portugal, Unipessoal, Lda

Identity

Trade Name
COUPLING MULTIFLEX 4H L FDA UDI
Generic Name
Pneumatic dental handpiece coupler FDA UDI
Device Name
Accessory connects micro-motors to the console or other boards, thus allowing the control and functioning of the whole device. FDA UDI
Model / Reference
1600902-001 FDA UDI
Description
Accessory connects micro-motors to the console or other boards, thus allowing the control and functioning of the whole device. FDA UDI

Identifiers

Catalog Number
1600902-001 FDA UDI
Primary DI / UDI-DI
J00716009020011 FDA UDI
FDA Product Code
EFB FDA UDI
GMDN Term
Pneumatic dental handpiece coupler 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: Pneumatic dental handpiece coupler

Coupling Multiflex 4h L by Bien-Air Portugal, Unipessoal, Lda — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pneumatic dental handpiece coupler.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f91e5fa6-7aff-441e-a20c-2e28f67ea4bf 35 fields · synced May 30, 2026