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Multi Tray

FDA UDI

Class I (US FDA UDI)

by Kettenbach GmbH & Co. KG

Identity

Trade Name
Multi Tray FDA UDI
Generic Name
Dental impression tray, single-use FDA UDI
Device Name
Multi Tray (Quandrant) FDA UDI
Model / Reference
17753 FDA UDI
Description
Multi Tray (Quandrant) FDA UDI

Identifiers

Catalog Number
17753 FDA UDI
Primary DI / UDI-DI
E217177531 FDA UDI
FDA Product Code
EHY FDA UDI
GMDN Term
Dental impression tray, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6880 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

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, single-use

Multi Tray by Kettenbach GmbH & Co. KG — 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

Sources (1)

  • FDA UDI 505e5d52-55f5-4700-b61e-1af593d8a030 34 fields · synced Jun 8, 2026