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Eurotray

FDA UDI

Class I (US FDA UDI)

by Plasdent Corp.

Identity

Trade Name
EUROTRAY FDA UDI
Generic Name
Dental impression tray, single-use FDA UDI
Device Name
#9 Impression Tray, Anterior, Light Blue FDA UDI
Model / Reference
ITE-ANT FDA UDI
Description
#9 Impression Tray, Anterior, Light Blue FDA UDI

Identifiers

Catalog Number
ITE-ANT FDA UDI
Primary DI / UDI-DI
D832ITEANT1 FDA UDI
FDA Product Code
EBH FDA UDI
GMDN Term
Dental impression tray, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3670 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: Dental impression tray, single-use

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

Similar devices

Also classified as Dental impression tray, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Plasdent Corp.

Sources (1)

  • FDA UDI b266a148-1440-4e37-beb9-7b0e3121a7b0 34 fields · synced Jun 1, 2026