← Back to catalogue

Dental Basics

FDA UDI

Class I (US FDA UDI)

by Dental Basics Inc.

Identity

Trade Name
Dental Basics FDA UDI
Generic Name
Dental material application tool, single-use FDA UDI
Device Name
Recycled Platsic Micro Applicators, Fine, Medium Green FDA UDI
Model / Reference
MA21 FDA UDI
Description
Recycled Platsic Micro Applicators, Fine, Medium Green FDA UDI

Identifiers

Primary DI / UDI-DI
00850061028112 FDA UDI
FDA Product Code
EJB FDA UDI
GMDN Term
Dental material application tool, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental material application tool, single-use

Dental Basics by Dental Basics Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental material application tool, single-use.

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
Dental Basics Inc.

Sources (1)

  • FDA UDI fcf8c150-1c66-4536-a3f3-f3a8eb970d7c 33 fields · synced May 30, 2026