Supra

FDA UDI

Class II (US FDA UDI)

by Jw North America, Inc.

Identity

Trade Name: SUPRA FDA UDI
Generic Name: Ultraviolet tanning device FDA UDI
Device Name: Ultraviolet tanning device FDA UDI
Model / Reference: Q-0800SI FDA UDI
Description: Ultraviolet tanning device FDA UDI

Identifiers

Catalog Number: 37015 FDA UDI
Primary DI / UDI-DI: G619370150 FDA UDI
FDA Product Code: LEJ FDA UDI
GMDN Term: Ultraviolet tanning device FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.4635 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

Yes

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

FDA UDI

Category: Ultraviolet tanning device

Supra by Jw North America, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 II	Pending data

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Manufacturer

Manufacturer: Jw North America, Inc.

Sources (1)

FDA UDI 5499484c-8bf5-45d1-8995-70e071d85e5b 34 fields · synced Sep 18, 2026