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: PROMETHEUS SELF CONTAINED LED SWIVEL COUPLER ADAPTS 4 HOLE TUBING TO 5 HOLE HANDPIECE FDA UDI
Model / Reference: PRO-4LEDQDS FDA UDI
Description: PROMETHEUS SELF CONTAINED LED SWIVEL COUPLER ADAPTS 4 HOLE TUBING TO 5 HOLE HANDPIECE FDA UDI

Identifiers

Catalog Number: PRO-4LEDQDS FDA UDI
Primary DI / UDI-DI: 00843471115435 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

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

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Also classified as Pneumatic dental handpiece coupler.

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Airlight — Beyes Dental Canada Inc · Class I
MK-dent Germany® — MK-Dent GmbH · Class I
Airlight — Beyes Dental Canada Inc · Class I
DENTALAIRE — Beyes Dental Canada Inc · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Young Innovations, Inc.

Sources (1)

FDA UDI 60571722-80fd-4e54-9088-ae184b503cfe 35 fields · synced May 30, 2026