← Back to catalogue

Garg

FDA UDI

Class I (US FDA UDI)

by Power Dental USA, Inc.

Identity

Trade Name
Garg FDA UDI
Generic Name
Periodontal hoe FDA UDI
Device Name
KRAMER NEVINES C36/37 FDA UDI
Model / Reference
G2004 FDA UDI
Description
KRAMER NEVINES C36/37 FDA UDI

Identifiers

Catalog Number
G2004 FDA UDI
Primary DI / UDI-DI
D943G20040 FDA UDI
FDA Product Code
EMQ FDA UDI
GMDN Term
Periodontal hoe FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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: Dressing/utility forceps, scissors-like, reusablePeriodontal hoe

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

Similar devices

Also classified as Periodontal hoe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Power Dental USA, Inc.

Sources (1)

  • FDA UDI 49a7c9d2-22bd-4901-8ea3-2bfd16d97e34 35 fields · synced May 30, 2026