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Within UL Solutions we provide a broad portfolio of offerings to all the medical device industries. This includes certification, Approved/Notified Body and consultancy services. In order to protect and prevent any conflict of interest, perception of conflict of interest and protection of both our brand and our customers brand, we have processes in place to identify and manage any potential conflicts of interest and maintain impartiality. UL Solutions is unable to provide consultancy services to EU MDD, MDR or IVDD Notified Body, UKCA MD Approved Body or MDSAP Customers.
  • Public Notice

UL Solutions Warns of Counterfeit Test Reports

The following is a notification from UL Solutions that the test reports identified below are counterfeit. They do not represent testing conducted by UL Solutions, and were not issued by UL Solutions.

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January 27, 2023

NORTHBROOK, ILLINOIS — Jan. 27, 2023The following is a notification from UL Solutions that the test reports identified below are counterfeit. They do not represent testing conducted by UL Solutions, and were not issued by UL Solutions.

Remedy:

UL Solutions recommends that these test reports be destroyed. The purported data and conclusions in the reports are fake and should not be used for any purpose.      

Identification of the reports: 

 Test for in vitro cytotoxicity: Elution method of AIVI FLEX ALIGNER AND RETAINER (Batch No.: 190820192-02) as per ISO 10993-5:2009(E) UL Project Number: 4789219021

The cover pages of the counterfeit test report is attached to this notice as Appendix A.

Skin sensitization test in guinea pigs (Guinea Pig Maximization Test) of AIVI FLEX ALIGNER AND RETAINER (Batch No.: 190820192 -02) as per ISO  10993-10:2010(E) UL Project Number: 4789219021

The cover pages of the counterfeit test report is attached to this notice as Appendix B.

Skin Irritation Test in New Zealand White Rabbits of AIVI FLEX ALIGNER AND RETAINER (Batch No.: 190820192 -02) as per ISO  10993-10:2010(E) UL Project Number: 4789219021

The cover pages of the counterfeit test report is attached to this notice as Appendix C.

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