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Enzymax Powder

FDA UDI

Class I (US FDA UDI)

by Hu-Friedy Mfg Co., Llc

Identity

Trade Name
Enzymax Powder FDA UDI
Generic Name
Medical device cleaning agent FDA UDI
Device Name
Enzymax Powder Ultrasonic Detergent and Presoak FDA UDI
Model / Reference
IMS-1230 FDA UDI
Description
Enzymax Powder Ultrasonic Detergent and Presoak FDA UDI

Identifiers

Primary DI / UDI-DI
10889950036348 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 Powder 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 ee10248e-3ee3-4eec-9ae7-c54f9fda9d38 35 fields · synced Jun 6, 2026