Maintenance Kit

FDA UDI

Class I (US FDA UDI)

by Zyris, Inc.

Identity

Trade Name: Maintenance Kit FDA UDI
Generic Name: Dental suction system FDA UDI
Device Name: Maintenance Kit, O-Ring, PVB, i3 FDA UDI
Model / Reference: AIL0241 FDA UDI
Description: Maintenance Kit, O-Ring, PVB, i3 FDA UDI

Identifiers

Catalog Number: AIL0241 FDA UDI
Primary DI / UDI-DI: 00810032660635 FDA UDI
FDA Product Code: EAZ FDA UDI
GMDN Term: Dental suction system FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.4630 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

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental suction system

Maintenance Kit by Zyris, 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: Zyris, Inc.

Sources (1)

FDA UDI fac1c858-3bae-4346-8569-9cec988780de 35 fields · synced Jun 1, 2026