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Image

FDA UDI

Class II (US FDA UDI)

by Kerr Corporation

Identity

Trade Name
Image FDA UDI
Generic Name
Alginate dental impression material FDA UDI
Device Name
DustFree Alginate Dental Impression Material Mint Sample Set Time: 3 Minutes FDA UDI
Model / Reference
ZB014 FDA UDI
Description
DustFree Alginate Dental Impression Material Mint Sample Set Time: 3 Minutes FDA UDI

Identifiers

Primary DI / UDI-DI
00814978021413 FDA UDI
510(k) Number
K160097 FDA UDI
FDA Product Code
ELW FDA UDI
GMDN Term
Alginate dental impression material FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3660 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Weight — 250 Gram FDA UDI

Category: Alginate dental impression material

Image by Kerr Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Alginate dental impression material.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kerr Corporation

Sources (1)

  • FDA UDI 059c38b7-7d2f-4299-89bc-ecb47b4805da 37 fields · synced Jun 8, 2026