← Back to catalogue

Maxill Maxset High Precision Alginate

FDA UDI

Class II (US FDA UDI)

by Maxill, Inc.

Identity

Trade Name
Maxill Maxset High Precision Alginate FDA UDI
Generic Name
Alginate dental impression material FDA UDI
Model / Reference
53776 FDA UDI

Identifiers

Primary DI / UDI-DI
00060705537768 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

Category: Alginate dental impression material

Maxill Maxset High Precision Alginate by Maxill, Inc. — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Maxill, Inc.

Sources (1)

  • FDA UDI c03f26af-37a8-4dce-8ad7-69e6de1b4edb 33 fields · synced May 30, 2026