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Plasdent

FDA UDI

Class I (US FDA UDI)

by Plasdent Corp.

Identity

Trade Name
Plasdent FDA UDI
Generic Name
X-ray film cassette holder FDA UDI
Device Name
VP Film Mount - 6H, 3 1/4" X 6 3/8" FDA UDI
Model / Reference
VP-6H FDA UDI
Description
VP Film Mount - 6H, 3 1/4" X 6 3/8" FDA UDI

Identifiers

Catalog Number
VP-6H FDA UDI
Primary DI / UDI-DI
D832VP6H1 FDA UDI
FDA Product Code
NRD FDA UDI
GMDN Term
X-ray film cassette holder 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: X-ray film cassette holder

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

Similar devices

Also classified as X-ray film cassette holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Plasdent Corp.

Sources (1)

  • FDA UDI 4bb09124-ff02-4ae0-b4c3-5cfb81eba9d9 34 fields · synced Jun 1, 2026