← Back to catalogue

Darby Dental Supply, LLC

FDA UDI

Class I (US FDA UDI)

by Darby Dental Supply, Llc

Identity

Trade Name
Darby Dental Supply, LLC FDA UDI
Generic Name
Diamond dental bur, single-use FDA UDI
Device Name
DIAMONDS FG 863-016XC FDA UDI
Model / Reference
5257073 FDA UDI
Description
DIAMONDS FG 863-016XC FDA UDI

Identifiers

Primary DI / UDI-DI
00889813062883 FDA UDI
FDA Product Code
DZP FDA UDI
GMDN Term
Diamond dental bur, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4535 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Diamond dental bur, reusableDiamond dental bur, single-use

Darby Dental Supply, LLC by Darby Dental Supply, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Diamond dental bur, single-use.

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

Manufacturer
Darby Dental Supply, Llc

Sources (1)

  • FDA UDI c4d6e746-7962-4bb4-bd6c-10c8c378c53e 33 fields · synced May 29, 2026