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Plasdent

FDA UDI

Class I (US FDA UDI)

by Plasdent Corp.

Identity

Trade Name
Plasdent FDA UDI
Generic Name
Bib/apron, adult, reusable FDA UDI
Device Name
Patient Barrier Apron, Knee Length, 27" X 48", Polyester, White FDA UDI
Model / Reference
PBA2748-1 FDA UDI
Description
Patient Barrier Apron, Knee Length, 27" X 48", Polyester, White FDA UDI

Identifiers

Catalog Number
PBA2748-1 FDA UDI
Primary DI / UDI-DI
D832PBA274810 FDA UDI
FDA Product Code
NRD FDA UDI
GMDN Term
Bib/apron, adult, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6640 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bib/apron, adult, reusable

Plasdent by Plasdent Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bib/apron, adult, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Plasdent Corp.

Sources (1)

  • FDA UDI 37ca9e4b-2914-4dd4-9d47-8dff23805557 34 fields · synced May 30, 2026