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Plasdent

FDA UDI

Class I (US FDA UDI)

by Plasdent Corp.

Identity

Trade Name
Plasdent FDA UDI
Generic Name
Dental impression material syringe, reusable FDA UDI
Device Name
Universal Material Carrier, Straight, Blue Ocean FDA UDI
Model / Reference
UCST-2P FDA UDI
Description
Universal Material Carrier, Straight, Blue Ocean FDA UDI

Identifiers

Catalog Number
UCST-2P FDA UDI
Primary DI / UDI-DI
D832UCST2P0 FDA UDI
FDA Product Code
EID FDA UDI
GMDN Term
Dental impression material syringe, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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: Dental impression material syringe, reusable

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

Similar devices

Also classified as Dental impression material syringe, 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 86190876-0f5e-49ff-9473-36063d077377 34 fields · synced May 30, 2026