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Intercept Plus

FDA UDI

Class I (US FDA UDI)

by Medivators Inc.

Identity

Trade Name
Intercept Plus FDA UDI
Generic Name
Medical device cleaning agent FDA UDI
Device Name
Intercept Plus Detergent is an alkaline, low foaming liquid detergent solution used in compatible AERs or for manual cleaning of immersible medical instruments. FDA UDI
Model / Reference
4002404 FDA UDI
Description
Intercept Plus Detergent is an alkaline, low foaming liquid detergent solution used in compatible AERs or for manual cleaning of immersible medical instruments. FDA UDI

Identifiers

Catalog Number
ML02-0145 FDA UDI
Primary DI / UDI-DI
40677964025929 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

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

Yes

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

Intercept Plus by Medivators 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
Medivators Inc.

Sources (1)

  • FDA UDI e43336b2-7eb7-4958-8ae8-325c169a0a27 35 fields · synced Jun 8, 2026