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Health-Tec/DHP High Volume Evacuation Tips

FDA UDI

Class I (US FDA UDI)

by Dental Health Products Inc

Identity

Trade Name
Health-Tec/DHP High Volume Evacuation Tips FDA UDI
Generic Name
Dental suction system cannula, single-use FDA UDI
Device Name
Health-Tec/DHP High Volume Evacuation Tips Non-Vented 50/bag FDA UDI
Model / Reference
540-HT2050 FDA UDI
Description
Health-Tec/DHP High Volume Evacuation Tips Non-Vented 50/bag FDA UDI

Identifiers

Catalog Number
540-HT2050 FDA UDI
Primary DI / UDI-DI
D773540HT20502 FDA UDI
FDA Product Code
EHZ FDA UDI
GMDN Term
Dental suction system cannula, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6640 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental suction system cannula, single-use

Health-Tec/DHP High Volume Evacuation Tips by Dental Health Products Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental suction system cannula, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c74167b8-7cc9-4ec0-b20d-98c5bba4c9c6 34 fields · synced May 30, 2026