← Back to catalogue

CaviWipes

FDA UDI

Class I (US FDA UDI)

by Metrex Research

Identity

Trade Name
CaviWipes FDA UDI
Generic Name
Medical device cleaning/disinfection wipe FDA UDI
Device Name
CAVIWIPES 2.0 12/CS FDA UDI
Model / Reference
14-1100 FDA UDI
Description
CAVIWIPES 2.0 12/CS FDA UDI

Identifiers

Primary DI / UDI-DI
00615375008768 FDA UDI
FDA Product Code
LRJ FDA UDI
GMDN Term
Medical device cleaning/disinfection wipe FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6890 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/disinfection wipe

CaviWipes by Metrex Research — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical device cleaning/disinfection wipe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Metrex Research

Sources (1)

  • FDA UDI 2b0f171c-1915-4cc5-85c0-579b1da4f79c 34 fields · synced May 31, 2026