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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
Pneumatic dental handpiece coupler FDA UDI
Device Name
FIBER OPTIC QUICK DISCONNECT SWIVEL FOR KAVO 5 HOLE FDA UDI
Model / Reference
W-KFOQDS FDA UDI
Description
FIBER OPTIC QUICK DISCONNECT SWIVEL FOR KAVO 5 HOLE FDA UDI

Identifiers

Catalog Number
W-KFOQDS FDA UDI
Primary DI / UDI-DI
00843471116159 FDA UDI
FDA Product Code
EFB FDA UDI
GMDN Term
Pneumatic dental handpiece coupler FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4200 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

No

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: Pneumatic dental handpiece coupler

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

Similar devices

Also classified as Pneumatic dental handpiece coupler.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 48294c97-34c4-4857-a3a0-e9e4a4e2d658 35 fields · synced Jun 8, 2026