Identity

Trade Name
JK FDA UDI
Generic Name
Ultraviolet tanning device FDA UDI
Device Name
UV - Tanning lamp FDA UDI
Model / Reference
Strahler JK 60/80 EF- Einzelv. FDA UDI
Description
UV - Tanning lamp FDA UDI

Identifiers

Catalog Number
8003 2000 FDA UDI
Primary DI / UDI-DI
04054657500358 FDA UDI
510(k) Number
K151674 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

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

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ultraviolet tanning device

Jk by G.L.E. Gesellschaft für lichttechnische Erzeugnisse mbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ultraviolet tanning device.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a1c50799-6e77-4477-83cb-7135d68a8e0b 37 fields · synced May 30, 2026