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Plasdent

FDA UDI

Class II (US FDA UDI)

by Plasdent Corp.

Identity

Trade Name
Plasdent FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
Digital Sensor Sleeves, #0/#1, 9"L X 1 3/4"W FDA UDI
Model / Reference
PS-00/01 FDA UDI
Description
Digital Sensor Sleeves, #0/#1, 9"L X 1 3/4"W FDA UDI

Identifiers

Catalog Number
PS-00/01 FDA UDI
Primary DI / UDI-DI
D832PS00011 FDA UDI
510(k) Number
K201604 FDA UDI
FDA Product Code
PEM FDA UDI
GMDN Term
Medical equipment/instrument drape, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medical equipment/instrument drape, single-use

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

Similar devices

Also classified as Medical equipment/instrument drape, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Plasdent Corp.

Sources (1)

  • FDA UDI d20e0106-4522-4768-b820-73104e9fdb77 35 fields · synced May 30, 2026