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CROMATIC 18 g

FDA UDI

Class II (US FDA UDI)

by Vannini Dental Industry Srl

Identity

Trade Name
CROMATIC 18 g FDA UDI
Generic Name
Alginate dental impression material FDA UDI
Device Name
Alginate for dental impressions FDA UDI
Model / Reference
002015 FDA UDI
Description
Alginate for dental impressions FDA UDI

Identifiers

Catalog Number
002015 FDA UDI
Primary DI / UDI-DI
08033712560267 FDA UDI
510(k) Number
K963609 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
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Total Volume — 27280 Milliliter FDA UDI

Category: Alginate dental impression material

CROMATIC 18 g by Vannini Dental Industry Srl — 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

Sources (1)

  • FDA UDI a2fce15a-e009-451c-a710-0aa7065f1e56 38 fields · synced Jun 1, 2026