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Garg

FDA UDI

Class II (US FDA UDI)

by Power Dental USA, Inc.

Identity

Trade Name
Garg FDA UDI
Generic Name
Dental suction system FDA UDI
Device Name
FRAZIER ASPIRATOR SUCTION TIP FRENCH STYLE WITH CONTROL RELIEF HOLE 4.0mm FDA UDI
Model / Reference
G6717 FDA UDI
Description
FRAZIER ASPIRATOR SUCTION TIP FRENCH STYLE WITH CONTROL RELIEF HOLE 4.0mm FDA UDI

Identifiers

Catalog Number
G6717 FDA UDI
Primary DI / UDI-DI
D943G67170 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
Dental suction system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical/emergency suction cannula, non-illuminating, reusableDental suction system

Garg by Power Dental USA, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental suction system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0c2cecb9-8803-4810-968a-53e96a8e24c9 35 fields · synced Jun 1, 2026