Health-Tec/DHP Hand Instruments

FDA UDI

Class I (US FDA UDI)

by Dental Health Products Inc

Identity

Trade Name: Health-Tec/DHP Hand Instruments FDA UDI
Generic Name: Dental spatula, reusable FDA UDI
Device Name: Health-Tec/DHP Cement Spatula Flexible 24A FDA UDI
Model / Reference: 700-1702 FDA UDI
Description: Health-Tec/DHP Cement Spatula Flexible 24A FDA UDI

Identifiers

Catalog Number: 700-1702 FDA UDI
Primary DI / UDI-DI: D77370017020 FDA UDI
FDA Product Code: GAF FDA UDI
GMDN Term: Dental spatula, 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Dental spatula, reusable

Health-Tec/DHP Hand Instruments by Dental Health Products Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Dental Health Products Inc

Sources (1)

FDA UDI beff4826-0b8e-4c0a-9715-fbfa18dc4431 34 fields · synced May 31, 2026