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KBL Tower Space 3000 hybridSun

FDA UDI

Class II (US FDA UDI)

by KBL GmbH

Identity

Trade Name
KBL Tower Space 3000 hybridSun FDA UDI
Generic Name
Ultraviolet tanning device FDA UDI
Device Name
This device is an over-the-counter device emitting ultraviolet light in the UVB and UVA region of the spectrum intended for tanning of the human skin of an adult person. FDA UDI
Model / Reference
T3/52-180 FDA UDI
Description
This device is an over-the-counter device emitting ultraviolet light in the UVB and UVA region of the spectrum intended for tanning of the human skin of an adult person. FDA UDI

Identifiers

Primary DI / UDI-DI
04260489020227 FDA UDI
510(k) Number
K151962 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ultraviolet tanning device

KBL Tower Space 3000 hybridSun by KBL GmbH — 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

Manufacturer
KBL GmbH

Sources (1)

  • FDA UDI 85e2d3dc-2078-420e-b09d-62df98680813 34 fields · synced May 29, 2026