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Health-Tec Barrier Film

FDA UDI

Class II (US FDA UDI)

by Dental Health Products Inc

Identity

Trade Name
Health-Tec Barrier Film FDA UDI
Generic Name
Instrument/equipment drape, single-use, non-sterile FDA UDI
Device Name
Health-Tec Barrier Film, 4" x 6", Clear FDA UDI
Model / Reference
660-HT46C FDA UDI
Description
Health-Tec Barrier Film, 4" x 6", Clear FDA UDI

Identifiers

Catalog Number
660-HT46C FDA UDI
Primary DI / UDI-DI
D773660HT46C1 FDA UDI
510(k) Number
K160232 FDA UDI
FDA Product Code
PEM FDA UDI
GMDN Term
Instrument/equipment drape, single-use, non-sterile 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Instrument/equipment drape, single-use, non-sterile

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

Similar devices

Also classified as Instrument/equipment drape, single-use, non-sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8d8e9bcd-e5f7-4548-ad5b-0f831cdf7d28 37 fields · synced May 30, 2026