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3D Dental

FDA UDI

Class I (US FDA UDI)

by 3d Dental Designs And Development, Llc

Identity

Trade Name
3D Dental FDA UDI
Generic Name
Dental matrix band, single-use FDA UDI
Device Name
Matrix Bands .002 144/Pk #3 FDA UDI
Model / Reference
MB02-3G FDA UDI
Description
Matrix Bands .002 144/Pk #3 FDA UDI

Identifiers

Catalog Number
MB02-3G FDA UDI
Primary DI / UDI-DI
00817169024767 FDA UDI
FDA Product Code
KQC FDA UDI
GMDN Term
Dental matrix band, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.1850 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

No

FDA UDI

Category: Dental matrix band, single-use

3D Dental by 3d Dental Designs And Development, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental matrix band, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5a98cdcf-6cdd-44d0-b555-6e7ff6d9ec4d 34 fields · synced May 30, 2026