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Johnson-Promident

FDA UDI

Class I (US FDA UDI)

by Young Innovations, Inc.

Identity

Trade Name
Johnson-Promident FDA UDI
Generic Name
Dental mandrel FDA UDI
Device Name
COMPOSITE DISC MANDREL RA PACK FDA UDI
Model / Reference
MAN-1958RA FDA UDI
Description
COMPOSITE DISC MANDREL RA PACK FDA UDI

Identifiers

Catalog Number
MAN-1958RA FDA UDI
Primary DI / UDI-DI
00843471121849 FDA UDI
FDA Product Code
EHJ FDA UDI
GMDN Term
Dental mandrel FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6010 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

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

Category: Dental mandrel

Johnson-Promident by Young Innovations, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental mandrel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ac7efcc6-2f15-4aaa-b6a4-f8803f22a25d 35 fields · synced May 30, 2026