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Garg

FDA UDI

Class I (US FDA UDI)

by Power Dental USA, Inc.

Identity

Trade Name
Garg FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
CASSETTES SURGICAL / UTILITY 7" L X 8" W X 1 1/4" D (174 X 203 X 31mm H) FDA UDI
Model / Reference
G7511 FDA UDI
Description
CASSETTES SURGICAL / UTILITY 7" L X 8" W X 1 1/4" D (174 X 203 X 31mm H) FDA UDI

Identifiers

Catalog Number
G7511 FDA UDI
Primary DI / UDI-DI
D943G75110 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Instrument tray, reusableDevice sterilization/disinfection container, reusable

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

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 431ae4ae-f051-435d-86fb-a1db4fb37865 35 fields · synced May 30, 2026