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PlastCare

FDA UDI

Class I (US FDA UDI)

by Proguard Health Inc.

Identity

Trade Name
PlastCare FDA UDI
Generic Name
Saliva absorbent FDA UDI
Device Name
3 Ply Proback European Bib 13" X 18" White FDA UDI
Model / Reference
PG-C125-DBW FDA UDI
Description
3 Ply Proback European Bib 13" X 18" White FDA UDI

Identifiers

Catalog Number
PG-C125-DBW FDA UDI
Primary DI / UDI-DI
D066PGC125DBW1 FDA UDI
FDA Product Code
KHR FDA UDI
GMDN Term
Saliva absorbent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6050 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: Saliva absorbent

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

Similar devices

Also classified as Saliva absorbent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e304ee8b-be19-4d45-90b5-db6f1672762c 34 fields · synced Jun 8, 2026