← Back to catalogue

DHP Universal Bond

FDA UDI

Class II (US FDA UDI)

by Dental Health Products Inc

Identity

Trade Name
DHP Universal Bond FDA UDI
Generic Name
Dentine bonding agent/set FDA UDI
Device Name
DHP Universal Bond Refill 5th Generation 5ml Bottle FDA UDI
Model / Reference
220-HT60B2 FDA UDI
Description
DHP Universal Bond Refill 5th Generation 5ml Bottle FDA UDI

Identifiers

Catalog Number
220-HT60B2 FDA UDI
Primary DI / UDI-DI
D773210HT60B20 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

No

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 Universal Bond 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

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

Manufacturer

Manufacturer
Dental Health Products Inc

Sources (1)

  • FDA UDI bd33c42b-730f-429a-a6bb-aaeffd05d0c7 35 fields · synced Jun 1, 2026