← Back to catalogue

Burkhart Dental Supply

FDA UDI

Class II (US FDA UDI)

by Burkhart Dental Supply Co., The

Identity

Trade Name
Burkhart Dental Supply FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
Core Build-Up Material Opaceous White - 25ml/48g FDA UDI
Model / Reference
72721963 FDA UDI
Description
Core Build-Up Material Opaceous White - 25ml/48g FDA UDI

Identifiers

Primary DI / UDI-DI
00810052618883 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3690 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

Dimensions & Sizes

Size
Weight — 48 Gram FDA UDI

Category: Dental composite resin

Burkhart Dental Supply by Burkhart Dental Supply Co., The — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

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

Sources (1)

  • FDA UDI a019eb41-9ba3-40c3-ab3d-1eb327568922 36 fields · synced Jun 1, 2026