A-dec

FDA UDI

Class I (US FDA UDI)

by A-Dec, Inc.

Identity

Trade Name: A-dec FDA UDI
Generic Name: Dental suction system FDA UDI
Device Name: Domestic Vacuum Tubings Kit,1 HVE,Gray3 FDA UDI
Model / Reference: 77.0514.01 FDA UDI
Description: Domestic Vacuum Tubings Kit,1 HVE,Gray3 FDA UDI

Identifiers

Catalog Number: 77.0514.01 FDA UDI
Primary DI / UDI-DI: 10194665002763 FDA UDI
FDA Product Code: EHZ FDA UDI
GMDN Term: Dental suction system 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

MRI Safety

MR Conditional FDA UDI

Category: Dental suction system

A-dec by A-Dec, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: A-Dec, Inc.

Sources (1)

FDA UDI a670013f-ef0d-47bb-b4ac-c157d22a8950 34 fields · synced May 29, 2026