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Alginelle

FDA UDI

Class II (US FDA UDI)

by Lascod Spa

Identity

Trade Name
ALGINELLE FDA UDI
Generic Name
Alginate dental impression material FDA UDI
Device Name
Orange alginate type 1 (450g) CATALOGUE NUMBER: - KAL102 = carton box containing n. 20 bags KAL001 FDA UDI
Model / Reference
KAL001 FDA UDI
Description
Orange alginate type 1 (450g) CATALOGUE NUMBER: - KAL102 = carton box containing n. 20 bags KAL001 FDA UDI

Identifiers

Catalog Number
KAL102 FDA UDI
Primary DI / UDI-DI
18016200010441 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

No

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

Category: Alginate dental impression material

Alginelle by Lascod Spa — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Alginate dental impression material.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lascod Spa

Sources (1)

  • FDA UDI 5e13fb43-9300-40f4-8c56-426b62bd5d25 35 fields · synced May 30, 2026