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Frost™ 37% Phosphoric Acid Etch 5ml

FDA UDI

Class II (US FDA UDI)

by Clinician's Choice Dental Products, Inc.

Identity

Trade Name
Frost™ 37% Phosphoric Acid Etch 5ml FDA UDI
Generic Name
Dental etching solution FDA UDI
Device Name
Dental Etchant FDA UDI
Model / Reference
345501 FDA UDI
Description
Dental Etchant FDA UDI

Identifiers

Catalog Number
345501 FDA UDI
Primary DI / UDI-DI
07540172009546 FDA UDI
FDA Product Code
EBF FDA UDI
JEW FDA UDI
GMDN Term
Dental etching solution FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3690 FDA UDI
872.6650 FDA UDI
Commercial Distribution
Not 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

Dimensions & Sizes

Size
Total Volume — 5 Milliliter FDA UDI

Frost™ 37% Phosphoric Acid Etch 5ml by Clinician's Choice Dental Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1fe14636-7940-403f-ba8f-61dd2a9c6676 38 fields · synced Jun 8, 2026