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MetriZyme

FDA UDI

Class I (US FDA UDI)

by Metrex Research

Identity

Trade Name
MetriZyme FDA UDI
Generic Name
Medical device-decontamination agent FDA UDI
Device Name
Dual Enzymatic Detergent FDA UDI
Model / Reference
10-4050 FDA UDI
Description
Dual Enzymatic Detergent FDA UDI

Identifiers

Primary DI / UDI-DI
00615375005729 FDA UDI
FDA Product Code
MNL FDA UDI
GMDN Term
Medical device-decontamination 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

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 5 Gallon FDA UDI

Category: Medical device-decontamination agent

MetriZyme by Metrex Research — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical device-decontamination agent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Metrex Research

Sources (1)

  • FDA UDI 3d66f87c-ce4d-4f3c-b057-ced7dff56bbd 36 fields · synced May 30, 2026