← Back to catalogue

Johnson-Promident

FDA UDI

Class I (US FDA UDI)

by Young Innovations, Inc.

Identity

Trade Name
Johnson-Promident FDA UDI
Generic Name
Carbide dental bur, reusable FDA UDI
Device Name
CARBIDE BUR HP#1 FDA UDI
Model / Reference
1HP-5 FDA UDI
Description
CARBIDE BUR HP#1 FDA UDI

Identifiers

Catalog Number
1HP-5 FDA UDI
Primary DI / UDI-DI
00843471102329 FDA UDI
FDA Product Code
EJL FDA UDI
GMDN Term
Carbide dental bur, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3240 FDA UDI
Commercial Distribution
Not 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

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Johnson-Promident by Young Innovations, Inc. — 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 0fdf8d0b-5901-4b77-aac1-b4fa42ef1ac1 36 fields · synced May 31, 2026