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Intercept Wipes

FDA UDI

Class I (US FDA UDI)

by Medivators Inc.

Identity

Trade Name
Intercept Wipes FDA UDI
Generic Name
Medical device cleaning agent FDA UDI
Model / Reference
ML02-0107 FDA UDI

Identifiers

Primary DI / UDI-DI
00677964036446 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

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

Yes

FDA UDI

Category: Medical device cleaning agent

Intercept Wipes 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 39bc620d-55c0-4d8f-bf0c-7a60b592b9f0 32 fields · synced May 30, 2026