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Freealgin

FDA UDI

Class II (US FDA UDI)

by Zhermack Spa

Identity

Trade Name
Freealgin FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Device Name
Addition silicone impression material FDA UDI
Model / Reference
C300110 FDA UDI
Description
Addition silicone impression material FDA UDI

Identifiers

Catalog Number
C300110 FDA UDI
Primary DI / UDI-DI
EZHIC3001101 FDA UDI
510(k) Number
K070700 FDA UDI
FDA Product Code
ELW FDA UDI
GMDN Term
Silicone 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

Yes

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
Total Volume — 100 Milliliter FDA UDI

Category: Silicone dental impression material

Freealgin by Zhermack Spa — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Silicone dental impression material.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zhermack Spa

Sources (1)

  • FDA UDI 7b50e87a-b667-4198-a413-5dd30be94a2b 37 fields · synced May 30, 2026