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FotoDent® tray2

FDA UDI

Class I (US FDA UDI)

by Dreve Dentamid GmbH

Identity

Trade Name
FotoDent® tray2 FDA UDI
Generic Name
Dental impression tray material FDA UDI
Device Name
No. FDA UDI
Model / Reference
D353001 FDA UDI
Description
No. FDA UDI

Identifiers

Catalog Number
D353001 FDA UDI
Primary DI / UDI-DI
E239D3530011 FDA UDI
FDA Product Code
EBH FDA UDI
GMDN Term
Dental impression tray material 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental impression tray material

FotoDent® tray2 by Dreve Dentamid GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental impression tray material.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dreve Dentamid GmbH

Sources (1)

  • FDA UDI 090e78c1-2664-49fc-9a07-ba86cc9a3a1b 36 fields · synced Jun 8, 2026