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Maxmicro

FDA UDI

Class I (US FDA UDI)

by Plasdent Corp.

Identity

Trade Name
MAXMICRO FDA UDI
Generic Name
Dental material application tool, single-use FDA UDI
Device Name
Applicators - 1.5mm, Fine, Yellow FDA UDI
Model / Reference
600-F-3 FDA UDI
Description
Applicators - 1.5mm, Fine, Yellow FDA UDI

Identifiers

Catalog Number
600-F-3 FDA UDI
Primary DI / UDI-DI
D832600F31 FDA UDI
FDA Product Code
KXF FDA UDI
GMDN Term
Dental material application tool, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6025 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental material application tool, single-use

Maxmicro by Plasdent Corp. — 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

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Manufacturer

Manufacturer
Plasdent Corp.

Sources (1)

  • FDA UDI 1c857797-026a-4f78-ac58-6b743e4ed0db 34 fields · synced Jun 8, 2026