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DHP Etch Gel

FDA UDI

Class II (US FDA UDI)

by Dental Health Products Inc

Identity

Trade Name
DHP Etch Gel FDA UDI
Generic Name
Dentine bonding agent/set FDA UDI
Device Name
DHP Etch Gel 4-1.2gm Syringes with 20 Tips FDA UDI
Model / Reference
220-100032 FDA UDI
Description
DHP Etch Gel 4-1.2gm Syringes with 20 Tips FDA UDI

Identifiers

Catalog Number
220-100032 FDA UDI
Primary DI / UDI-DI
D7732201000321 FDA UDI
FDA Product Code
KLE FDA UDI
GMDN Term
Dentine bonding agent/set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3200 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

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dentine bonding agent/set

DHP Etch Gel by Dental Health Products Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dentine bonding agent/set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dental Health Products Inc

Sources (1)

  • FDA UDI 747b9664-68fd-4813-8ff8-03453a16d7ce 35 fields · synced May 30, 2026