Diamond Logo
Diamond Logo
Diamond Refurb BannerAlfa Wassermann ACE

ACE, ACEAlera, Axcel, NExCt, VetACE


  • Direct, Drop-in Replacement Products
  • 2-3 Years Expiration on all Reagents
  • FDA 510k Cleared, ISO Certified, CE Marked
  • Prompt Same Day Shipping



Cal A Solution

Cal A Solution

Item# AW-SA1029D

Cal A Solution for Alfa Wassermann ACE, VetACE, NeXCt, Alera

Cl- Electrode

Cl- Electrode

Item# AW-906178D

Cl- Electrode for Alfa Wassermann Chemistry ISE Modules

K+ Electrode

K+ Electrode

Item# AW-903394D

K+ Electrode for Alfa Wassermann Chemistry ISE Modules

Na+ Electrode

Na+ Electrode

Item# AW-903393D

Na+ Electrode for Alfa Wassermann Chemistry ISE Modules

Peristaltic Pump Tubing

Peristaltic Pump Tubing

Item# AW-906182D

Peristaltic Pump Tubing for Alfa Wassermann ACE, Alera, NExCt, VEtACE

Reference Electrode

Reference Electrode

Item# AV-BP5026D

Reference Electrode. For use Diamond SmartLyte, Carelyte, Alfa Wassermann Starlyte III, Starlyte V, Idexx Vetlyte, Roche 9110, 9120, 9130, 9140, 9180, 9181 and Alfa Wassermann Chemistry ISE Systems, Bayer Opera

Reference Electrode Housing

Reference Housing for Alfa Wassermann Chemistry ISE Modules

Reference Solution

Reference Solution

Item# AV-BP0095D

Reference Solution (3x90mL) for AVL 98x and Alfa Wasserman ISE Modules

Sample Probe

Sample Probe

Item# AW-402377D

Sample Probe for Alfa Wassermann ACE, Alera, NExCt, VEtACE

Standard B

Standard B

Item# AV-BP0442D

System Diluent

System Diluent

Item# AW-SA1021D

System Diluent for Alfa Wassermann ACE, VetACE, NeXCt, Alera

ISO
ISO
Facebook
Instagram
Contact Us

Corporate Headquarters (USA)
Diamond Diagnostics Inc.
333 Fiske Street
Holliston, MA 01746-2048
Tel: +1 508.429.0450

Distribution Center (EU)
Diamond Diagnostics Kft.
1044 Budapest, Hungary
Óradna Street 6
Tel: +36 (1) 787 2222

Quality

ISO 9001:2015 (US)
ISO 9001:2015 (EU)
ISO 13485:2016 (US)
ISO 13485:2016 (EU)

Diamond Diagnostics Inc. is registered with the United States Food and Drug Administration as an Initial Importer Manufacturer and Contract Manufacturer. Establishment registration and device listing can be found under ID: 3003030793.

Diamond has been registered with the Food and Drug Administration since 2001 and regulated by its cGMP system requirements.

All products manufactured by Diamond carry the necessary FDA clearance and comply to the European Union IVD Directive. Every department and function in our company is standardized, controlled and routinely audited.

FDA logo

The names and logos of manufacturers, their instruments, and their products referred to herein may be protected by trademark or other law, and are used herein solely for purpose of reference. Products are available for international distribution only unless otherwise indicated. Diamond Diagnostics expressly disclaims any affiliation with products it does not manufacture, as well as sponsorship by other manufacturers. For current regulatory status on products within this website, please contact your sales representative. Prices and Information shown are for reference only and may change without notice. SmartLyte®, ProLyte®, CareLyte®, and Down-To-Frame® Refurbishing are Registered Trademarks of Diamond Diagnostics®.

©2021 Diamond Diagnostics®All Rights Reserved.