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Enzymax PAX

FDA UDI

Class I (US FDA UDI)

by Hu-Friedy Mfg Co., Llc

Identity

Trade Name
Enzymax PAX FDA UDI
Generic Name
Medical device cleaning agent FDA UDI
Device Name
Enzymax PAX Ultrasonic Detergent and Presoak Powder FDA UDI
Model / Reference
IMS-1232 FDA UDI
Description
Enzymax PAX Ultrasonic Detergent and Presoak Powder FDA UDI

Identifiers

Primary DI / UDI-DI
10889950036355 FDA UDI
FDA Product Code
FLG FDA UDI
GMDN Term
Medical device cleaning agent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6150 FDA UDI
Commercial Distribution
Not 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Enzymax PAX by Hu-Friedy Mfg Co., Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5ccf5d50-30e8-4d1e-a604-7f9362c09c68 35 fields · synced May 31, 2026