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Tur Prestige L

FDA UDI

Class I (US FDA UDI)

by Bien-Air Portugal, Unipessoal, Lda

Identity

Trade Name
Tur Prestige L FDA UDI
Generic Name
Dental surgical power tool motorized handpiece/set, pneumatic FDA UDI
Device Name
Turbines are intended to generate rotating mechanical energy from compressed air FDA UDI
Model / Reference
1600380-001 FDA UDI
Description
Turbines are intended to generate rotating mechanical energy from compressed air FDA UDI

Identifiers

Catalog Number
1600380-001 FDA UDI
Primary DI / UDI-DI
J00716003800011 FDA UDI
FDA Product Code
EFB FDA UDI
GMDN Term
Dental surgical power tool motorized handpiece/set, pneumatic 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental surgical power tool motorized handpiece/set, pneumatic

Tur Prestige L by Bien-Air Portugal, Unipessoal, Lda — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental surgical power tool motorized handpiece/set, pneumatic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bien-Air Portugal, Unipessoal, Lda

Sources (1)

  • FDA UDI d94af054-2e6b-4bae-a473-4fb17a91c4bc 35 fields · synced May 30, 2026