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Maxizyme Tablets

FDA UDI

Class I (US FDA UDI)

by Henry Schein, Inc.

Identity

Trade Name
Maxizyme Tablets FDA UDI
Generic Name
Medical device cleaning agent FDA UDI
Device Name
Maxizyme Enzymatic Ultrasonic Cleaning Tablets FDA UDI
Model / Reference
9000475 FDA UDI
Description
Maxizyme Enzymatic Ultrasonic Cleaning Tablets FDA UDI

Identifiers

Catalog Number
9000475 FDA UDI
Primary DI / UDI-DI
00304040028896 FDA UDI
FDA Product Code
MNL FDA UDI
GMDN Term
Medical device cleaning agent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1500 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Medical device cleaning agent

Maxizyme Tablets by Henry Schein, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical device cleaning agent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Henry Schein, Inc.

Sources (1)

  • FDA UDI abbc301f-909c-489b-a9be-7607316e7130 34 fields · synced Jun 8, 2026