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Prevantics® Device Large Swab

FDA UDI

Class U (US FDA UDI)

by Professional Disposables International, Inc.

Identity

Trade Name
Prevantics® Device Large Swab FDA UDI
Generic Name
Medical device cleaning/disinfection wipe FDA UDI
Device Name
Pre-moistened swab to disinfect needleless access sites prior to use. FDA UDI
Model / Reference
C71200 FDA UDI
Description
Pre-moistened swab to disinfect needleless access sites prior to use. FDA UDI

Identifiers

Catalog Number
C71200 FDA UDI
Primary DI / UDI-DI
00310819000031 FDA UDI
510(k) Number
K132380 FDA UDI
FDA Product Code
LKB FDA UDI
GMDN Term
Medical device cleaning/disinfection wipe FDA UDI

Classification

Device Class
U 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 0.040 Fluid Ounce FDA UDI

Category: Medical device cleaning/disinfection wipe

Prevantics® Device Large Swab by Professional Disposables International, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical device cleaning/disinfection wipe.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 43860018-0782-419b-964d-835e9dfd26f1 38 fields · synced Jun 8, 2026