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Dental City

FDA UDI

Class I (US FDA UDI)

by Icp, Inc.

Identity

Trade Name
Dental City FDA UDI
Generic Name
Dental suction system cannula, single-use FDA UDI
Device Name
HVE Combo Vented & Non-Vented - White 100/Bag FDA UDI
Model / Reference
62-300C FDA UDI
Description
HVE Combo Vented & Non-Vented - White 100/Bag FDA UDI

Identifiers

Primary DI / UDI-DI
D77162300C1 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

Yes

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

No

FDA UDI

Category: Dental suction system cannula, single-use

Dental City by Icp, 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

Manufacturer
Icp, Inc.

Sources (1)

  • FDA UDI 6ebc2ebb-52f6-42e9-87aa-69df214f3d68 33 fields · synced May 30, 2026