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 - 4H3V, 2 1/2" X 11 1/4" FDA UDI
Model / Reference: VP-4H3V FDA UDI
Description: VP Film Mount - 4H3V, 2 1/2" X 11 1/4" FDA UDI

Identifiers

Catalog Number: VP-4H3V FDA UDI
Primary DI / UDI-DI: D832VP4H3V1 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

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.

QT-LCH — CARESTREAM HEALTH, INC. · Class I
SEDECAL — Sedecal., Sa. · Class I
Mindray — Nanjing Mindray Bio-Medical Electronics Co., Ltd · Class I
dose-map™ — Ashland Specialty Ingredients, G.P. · Class II
Q-DRT-DRXT-R — CARESTREAM HEALTH, INC. · Class II
OPERON — STRYKER Communications, Inc. · Class I
LLD 129 Compact — Drtech Corp. · Class I
dose-map™ — Ashland Specialty Ingredients, G.P. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Plasdent Corp.

Sources (1)

FDA UDI 0725f852-c960-443b-a5d4-fbf4437d9841 34 fields · synced May 30, 2026