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Health-Tec/DHP Barrier Products

FDA UDI

Class II (US FDA UDI)

by Dental Health Products Inc

Identity

Trade Name
Health-Tec/DHP Barrier Products FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
Health-Tec/DHP Barrier Film 4" x 6" Blue 1200/box FDA UDI
Model / Reference
660-HT46B2 FDA UDI
Description
Health-Tec/DHP Barrier Film 4" x 6" Blue 1200/box FDA UDI

Identifiers

Catalog Number
660-HT46B2 FDA UDI
Primary DI / UDI-DI
D773660HT46B21 FDA UDI
FDA Product Code
PEM FDA UDI
GMDN Term
Medical equipment/instrument drape, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medical equipment/instrument drape, single-use

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

Similar devices

Also classified as Medical equipment/instrument drape, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 013ce843-c6f3-4eb3-8247-9c1edcabc48e 34 fields · synced Jun 8, 2026