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Sign in to claim this brandAGILENT TECHNOLOGIES SINGAPORE PTE LTD
US
Last updated May 24, 2026
What AGILENT TECHNOLOGIES SINGAPORE PTE LTD makes
Agilent Technologies Singapore Pte Ltd manufactures in vitro diagnostic (IVD) antibodies and related reagents, including cytokeratin IVD antibodies, kappa/lambda light chain immunoglobulin IVD antibodies, and various cell marker IVD antibodies such as CD3, CD4, CD8, CD34, CD45, and CD68. The company also produces microscope slide stainers IVD and associated accessories like Dako Omnis DI Water Filling Accessories for use in laboratory testing.
The manufacturer's devices are classified as Class I, Class II, and Class III medical devices and are listed in the FDA's Unique Device Identification (FDA UDI) system. Agilent Technologies Singapore Pte Ltd is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What does Agilent Technologies Singapore Pte Ltd manufacture?
Agilent Technologies Singapore Pte Ltd manufactures in vitro diagnostic (IVD) antibodies and related reagents, including cytokeratin IVD antibodies, kappa/lambda light chain immunoglobulin IVD antibodies, and various cell marker IVD antibodies such as CD3, CD4, CD8, CD34, CD45, and CD68. The company also produces microscope slide stainers IVD and associated accessories like Dako Omnis DI Water Filling Accessories for use in laboratory testing.
Where is Agilent Technologies Singapore Pte Ltd based?
Agilent Technologies Singapore Pte Ltd is based in the United States. The company operates from its headquarters in the US, where it develops and manufactures its diagnostic products and laboratory equipment.
Which regulatory registries list Agilent Technologies Singapore Pte Ltd's devices?
Agilent Technologies Singapore Pte Ltd's devices are listed in the FDA's Unique Device Identification (FDA UDI) system. This registry provides information about medical devices, including their identification, manufacturing details, and classification status.
How are Agilent Technologies Singapore Pte Ltd's devices classified?
Agilent Technologies Singapore Pte Ltd's devices are classified as Class I, Class II, and Class III medical devices. Class I devices pose the lowest risk, Class II devices require more regulatory controls, and Class III devices support or sustain human life and may present potential unreasonable risk of illness or injury.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- agilent.com
- —
- —
- [email protected]
- Phone
- +4544859500
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 894671143
Catalogue (557)
Page 12 of 12| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Mono Mo A-Hu Cytokeratin 20 Cl Ks20.8 | M7019 | FDA UDI | Class I | Active |
| Mono Mo A-Hu Cytokeratin Cl MNF116 | M0821 | FDA UDI | Class I | Active |
| Mono Mo A-Hu Desmin Cl D33 | M0760 | FDA UDI | Class I | Active |
| Mono Mo A-Hu Hepatocyte Cl OCH1E5 | M7158 | FDA UDI | Class I | Active |
| FLEX Mono Mo A-Hu CD68 Cl PG-M1 RTU (Dako Omnis) | GA613 | FDA UDI | Class I | Active |
| Dako | M0751 | FDA UDI | Class I | Unknown |
| FLEX Mono Mo A-Hu p63 Protein Cl DAK-p63 Ready-to-Use (Dako Omnis) | GA662 | FDA UDI | Class I | Active |
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