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PlastCare

FDA UDI

Class I (US FDA UDI)

by Proguard Health Inc.

Identity

Trade Name
PlastCare FDA UDI
Generic Name
General-purpose absorbent tip applicator/swab, single-use FDA UDI
Device Name
6" Cotton Tipped Applicator FDA UDI
Model / Reference
PG-CTA-006 FDA UDI
Description
6" Cotton Tipped Applicator FDA UDI

Identifiers

Catalog Number
PG-CTA-006 FDA UDI
Primary DI / UDI-DI
D066PGCTA0061 FDA UDI
FDA Product Code
KXF FDA UDI
GMDN Term
General-purpose absorbent tip applicator/swab, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6025 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

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: General-purpose absorbent tip applicator/swab, single-use

PlastCare by Proguard Health Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose absorbent tip applicator/swab, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a299cce9-df30-45fc-9e6f-33e717c7b1dc 34 fields · synced May 30, 2026