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3m™

FDA UDI

Class II (US FDA UDI)

by 3m Company

Identity

Trade Name
3M™ FDA UDI
Generic Name
Dental etching solution FDA UDI
Device Name
3M™ ESPE™ Etching Liquid, 1923 FDA UDI
Model / Reference
1923 FDA UDI
Description
3M™ ESPE™ Etching Liquid, 1923 FDA UDI

Identifiers

Catalog Number
1923 FDA UDI
Primary DI / UDI-DI
30605861032798 FDA UDI
FDA Product Code
KLE FDA UDI
GMDN Term
Dental etching solution FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3200 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: Dental etching solution

3m™ by 3m Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental etching solution.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3m Company

Sources (1)

  • FDA UDI 03243c3c-e392-411d-b2df-2a8a206bdf47 35 fields · synced May 29, 2026