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ET Foam

FDA UDI

Class I (US FDA UDI)

by Germiphene Corp.

Identity

Trade Name
ET Foam FDA UDI
Generic Name
Medical device cleaning agent FDA UDI
Device Name
ET Foam - 946 mL FDA UDI
Model / Reference
TRANS-FOAM FDA UDI
Description
ET Foam - 946 mL FDA UDI

Identifiers

Catalog Number
TRANS-FOAM FDA UDI
Primary DI / UDI-DI
00850046436338 FDA UDI
FDA Product Code
JCB FDA UDI
GMDN Term
Medical device cleaning agent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4010 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

No

FDA UDI

Category: Medical device cleaning agent

ET Foam by Germiphene Corp. — 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
Germiphene Corp.

Sources (1)

  • FDA UDI 60d8b403-6161-4db2-876f-8b7b26b50592 35 fields · synced May 31, 2026