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Contact Matrix

FDA UDI

Class I (US FDA UDI)

by Danville Materials, Llc

Identity

Trade Name
CONTACT MATRIX FDA UDI
Generic Name
Dental matrix band, reusable FDA UDI
Device Name
MEGA,V,CLINICAL KIT FDA UDI
Model / Reference
94272 FDA UDI
Description
MEGA,V,CLINICAL KIT FDA UDI

Identifiers

Catalog Number
94272 FDA UDI
Primary DI / UDI-DI
00816594022065 FDA UDI
FDA Product Code
EIG FDA UDI
GMDN Term
Dental matrix band, reusable 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental matrix band, reusable

Contact Matrix by Danville Materials, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental matrix band, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d7b0650d-406f-4963-b5fe-ea9d1ee5253c 35 fields · synced Jun 7, 2026