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Sign in to claim this brandHach Company
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 100 DAYTON AVE., AMES, IA, 50010
- Website
- hach.com
- —
- —
- [email protected]
- Phone
- 800-227-4224
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 1000518597
- DUNS Number
- 091381780
Catalogue (23)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Hach | 9638600 | FDA UDI | Class II | Active |
| Hach | 9756600 | FDA UDI | Class II | Active |
| SteriChek® Blood Leak Reagent Strips | 812014 | FDA UDI | Class II | Unknown |
| Sterichek® BiCarb pH Reagent Strips | 811916 | FDA UDI | Class II | Unknown |
| SteriChek® Blood Leak Reagent Strips | 812014 | FDA UDI | Class II | Unknown |
| Hach | 9717300 | FDA UDI | Class II | Active |
| SteriChek® Residual Chlorine Reagent Strips | 811900 | FDA UDI | Class II | Unknown |
| SteriChek® Peroxide Reagent Strips | 811905 | FDA UDI | Class II | Unknown |
| Stericide Peroxide Reagent Strips | 811905B | FDA UDI | Class II | Unknown |
| Hach | 9746600 | FDA UDI | Class II | Active |
| Hach | 9747300 | FDA UDI | Class II | Active |
| Hach | 9638900 | FDA UDI | Class II | Active |
| SteriChek® Total Chlorine Test Kit | 811902 | FDA UDI | Class II | Unknown |
| Hach | 9747400 | FDA UDI | Class II | Active |
| SteriChek® Residual Peroxide Reagent Strips | 811905 | FDA UDI | Class II | Unknown |
| Hach | 9747500 | FDA UDI | Class II | Active |
| SteriChek® Peracetic Acid Reagent Strips | 811906 | FDA UDI | Class II | Unknown |
| Sterichek® Total Chlorine Test Kit Refill | 811902 | FDA UDI | Class II | Unknown |
| Hach | 9730100 | FDA UDI | Class II | Active |
| Hach CM130 Chlorine Monitoring System | K162471 | FDA 510(k) | Class II | Active |
| Opaciden Opa Reagent Strips | K070419 | FDA 510(k) | Class II | Active |
| Sterichek Glutaraldehyde Reagent Strips | K040660 | FDA 510(k) | Class II | Active |
| Sterichek Blood Leak Reagent Strips | K042322 | FDA 510(k) | Class II | Active |
Related Companies
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FDA Recalls (5)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Apr 21, 2009 | Z-2016-2009 | — | terminated | Some of the reagent strip bottles contain the incorrect strips |
| May 23, 2008 | Z-2354-2008 | — | terminated | Inconsistencies in total chlorine and free chlorine levels may result in providing inaccurate false positive or false negative results |
| May 23, 2008 | Z-2352-2008 | — | terminated | Inconsistencies in total chlorine and free chlorine levels may result in providing inaccurate false positive or false negative results |
| May 23, 2008 | Z-2355-2008 | — | terminated | Inconsistencies in total chlorine and free chlorine levels may result in providing inaccurate false positive or false negative results |
| May 23, 2008 | Z-2353-2008 | — | terminated | Inconsistencies in total chlorine and free chlorine levels may result in providing inaccurate false positive or false negative results |