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First Quarter

FDA UDI

Class II (US FDA UDI)

by Danville Materials, Llc

Identity

Trade Name
FIRST QUARTER FDA UDI
Generic Name
Polyether dental impression material FDA UDI
Device Name
IST QTR,MONO,FS,CHOC/MINT,ECON FDA UDI
Model / Reference
90902 FDA UDI
Description
IST QTR,MONO,FS,CHOC/MINT,ECON FDA UDI

Identifiers

Catalog Number
90902 FDA UDI
Primary DI / UDI-DI
00816594021167 FDA UDI
FDA Product Code
ELW FDA UDI
GMDN Term
Polyether 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

Yes

FDA UDI

Category: Polyether dental impression material

First Quarter by Danville Materials, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyether dental impression material.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5cc0bfdd-7cb4-4d6a-b830-c41da24c382d 36 fields · synced May 30, 2026