CERTIFICATE

Number: 2110823 CE08

CE MARKING OF CONFORMITY
MEDICAL DEVICES

Issued to:
Velab, Co.
1431 West Polk Ave.
Pharr, TX 78577
USA
For the product category:

Balances, Centrifuges, Microscopes and Spectrophotometers

KEMA grants the right to use the EC Notified Body Indentification Numner illustated below to
accompany the CE Making of Conformity on the products concerned conforming to the required
Technics Documenta-tion and meeting the provisions of the EC-Directive which apply to them:

0348
Documentos, that form the basis of this certificate:
Certification Notices 2110821CN, initially dated February 27, 2019
Addendum, initially dated February 27, 2019

KEMA hereby declares that the above mentiones manufacturer fullils the relevant provision of “Besluit Medische Hulpmiddelen” the
Dutch tranposition of the Directive 93/42EEC of June 14, 1993 concerning medical devices, including all subsequent amendments,
and that for the above mentiones product category the Conformity Assesment Procedure Annex II, section 3 for Class lla products,
is executed bye the Manufacturer in accordance with the provisions of the Council DIrective 93/42/EEC of June 14, 1993.
The necessary information and the reference to the relevant documentation, of the products concerned and the assessments
performed, are started in the Certification Notice which forms and integrtive part of this certificate.

This certificate is valid until: December 1, 2022

Issued for the first time: February 27, 2019

drs G.J. Zoetbrood dr. ir. G.W. Bos

Managing Director Certification Manager

©Integral publication of this certiÿcate is allowed.

KEMA Medical
KEMA Quality B.V Ultrechetseweg 310, 6812 AR Amhem P.O Box 5185, 6802 ED Amhem The Netherlands
T +31 26 3 56 20 00 F +31 26 3 52 58 00 costumer@kema.com www.kema.com Registered Amhem 06085396