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ICE Build Up Liquid

FDA UDI

Class II (US FDA UDI)

by Zirkonzahn GmbH

Identity

Trade Name
ICE Build Up Liquid FDA UDI
Generic Name
Dental articulation paste/solution FDA UDI
Device Name
Content: 50 ml For mixing ceramic powders FDA UDI
Model / Reference
KEAA4301 FDA UDI
Description
Content: 50 ml For mixing ceramic powders FDA UDI

Identifiers

Primary DI / UDI-DI
D800KEAA4301 FDA UDI
FDA Product Code
EIH FDA UDI
GMDN Term
Dental articulation paste/solution FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.6660 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental articulation paste/solution

ICE Build Up Liquid by Zirkonzahn GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental articulation paste/solution.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zirkonzahn GmbH

Sources (1)

  • FDA UDI e24a0805-10c8-49f2-a996-2ad3a2d923d8 34 fields · synced May 30, 2026