Skip to content

Cosmolux Lynx FR71 / Cosmolux Lynx K2 / 200W / SM

by NARVA Lichtquellen GmbH + Co KG.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04014501005408 UDI-DI Date23 Sep 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Cosmolux Lynx
Generic Name
Ultraviolet tanning device
Model / Ref / Catalog
FR71 / Cosmolux Lynx K2 / 200W / SM, 26504
Primary DI / UDI-DI
04014501005408
FDA Product Code
LEJ
GMDN Term
Ultraviolet tanning device
Device Class
Class II
Regulation Number
878.4635
GUDID distribution status
In Commercial Distribution

Other devices from NARVA Lichtquellen GmbH + Co KG.

See all devices from NARVA Lichtquellen GmbH + Co KG. →

Properties

  • Over-the-Counter
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No