← Back to catalogue

Burkhart Dental Supply

FDA UDI

Class I (US FDA UDI)

by Burkhart Dental Supply Co., The

Identity

Trade Name
Burkhart Dental Supply FDA UDI
Generic Name
Diamond dental bur, reusable FDA UDI
Device Name
856L-018C Coarse FG Diamond (25) FDA UDI
Model / Reference
72722124 FDA UDI
Description
856L-018C Coarse FG Diamond (25) FDA UDI

Identifiers

Primary DI / UDI-DI
00815878025907 FDA UDI
FDA Product Code
DZP FDA UDI
GMDN Term
Diamond dental bur, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4535 FDA UDI
Commercial Distribution
Not 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

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

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 abbef767-e32d-4f1b-8e1d-895e3a293908 35 fields · synced May 31, 2026