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Sign in to claim this brandARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD.
US
Last updated May 24, 2026
What ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD. makes
The company manufactures medical devices for critical care monitoring and vascular access, including invasive blood pressure monitoring systems such as tubing sets, transducer sets, and single-use pressure transducers. It also produces vascular catheter introduction sets, pulmonary artery balloon catheters with electrical components, and reusable connection cables for medical devices. Additional products include blood pressure transducer holders, pressure transducer domes, and multi-lumen catheters for various clinical applications.
All listed devices fall under Class II regulatory classification in the US, with product authorisation via the FDA’s UDI (Unique Device Identifier) system. The company’s portfolio is registered under the FDA’s UDI database, ensuring traceability and compliance with US medical device regulations. The manufacturer operates from 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 types of medical devices does Argon Critical Care Systems Singapore Pte. Ltd. manufacture?
Argon Critical Care Systems Singapore Pte. Ltd. specializes in devices for critical care and vascular access. Its portfolio includes invasive blood pressure monitoring systems like tubing sets, transducer sets, and single-use pressure transducers. The company also produces vascular catheter introduction sets, pulmonary artery balloon catheters with electrical components, reusable connection cables, blood pressure transducer holders, and multi-lumen catheters. These products support monitoring and fluid management in clinical settings.
Where is Argon Critical Care Systems Singapore Pte. Ltd. based?
The company is based in the United States. While its name includes 'Singapore,' the operational headquarters and manufacturing are located in the US, aligning with its regulatory filings and device listings.
Which regulatory registries list Argon Critical Care Systems Singapore Pte. Ltd.’s devices?
The company’s devices are registered under the FDA’s UDI (Unique Device Identifier) system. This database ensures traceability and compliance with US medical device regulations, allowing healthcare providers and regulators to identify and track its products.
How are Argon Critical Care Systems Singapore Pte. Ltd.’s devices classified in the US?
All of Argon Critical Care Systems Singapore Pte. Ltd.’s listed devices fall under Class II regulatory classification in the US. This classification applies to devices that generally pose moderate risk and require special controls to ensure safety and effectiveness, such as performance standards or post-market surveillance.
Why are Argon Critical Care Systems Singapore Pte. Ltd.’s devices authorised via the FDA’s UDI system?
The FDA’s UDI system assigns a unique identifier to each medical device to improve tracking, reduce medical errors, and enhance supply chain efficiency. Since Argon’s devices are Class II, they require this identification to ensure compliance with US regulations and facilitate transparency in healthcare settings. The UDI system helps streamline device recall processes and verify product authenticity.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- argonmedical.com
- —
- —
- [email protected]
- Phone
- 1.800.927.4669
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 595138793
Catalogue (546)
Page 5 of 11| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Tc-Mq-1 Dts Intfc Ca Marquette W/Neg Cal | 684096 | FDA UDI | Class II | Active |
| Merit Medical® | 10884450325190 | FDA UDI | Class II | Active |
| Umm | 682104 | FDA UDI | Class II | Active |
| Dtx(tm) Plus Dt-Dl60 | 682028 | FDA UDI | Class II | Active |
| Safedraw™ | 10884450372941 | FDA UDI | Class II | Active |
| Safedraw™ | 10884450326593 | FDA UDI | Class II | Active |
| Careflow(tm) 1 Lumen 2.5fr X 200mm | 681633 | FDA UDI | Class II | Active |
| Ta2101 Angiographic Manifold | 682138 | FDA UDI | Class II | Active |
| Safedraw™ | 10884450372804 | FDA UDI | Class II | Active |
| Ta2100 Angiographic Manifold | 682110 | FDA UDI | Class II | Active |
| Careflow(tm) 5 Lumen 9.5fr X 150mm | 681736 | FDA UDI | Class II | Active |
| Tc-Nk Dts Intfc Ca Nihon Kohden | 684090 | FDA UDI | Class II | Active |
| Tc-Shi-2 Dts Intfc Ca Shiley | 684139 | FDA UDI | Class II | Active |
| P23xl™ | 10884450323189 | FDA UDI | Class II | Active |
| Spc-4(4-Way Stopcock) | 682097 | FDA UDI | Class II | Active |
| Comp Prline Mf 175cm Clr | 682231 | FDA UDI | Class II | Active |
| Safedraw(tm) Dt-6012sdt | 682143 | FDA UDI | Class II | Active |
| Careflow(tm) Ultra Basic 1 Lumen 16g X 200mm | 681667 | FDA UDI | Class II | Active |
| Dtx(tm) Plus Dt-6012 | 682014 | FDA UDI | Class II | Active |
| Critikit™ | 10884450557102 | FDA UDI | Class II | Active |
| Merit Medical® | 10884450325329 | FDA UDI | Class II | Active |
| Tc-Fk-Ds3300 Dts Intfc Ca Fukuda Dynascope | 684150 | FDA UDI | Class II | Active |
| Careflow(tm) Ultra Basic 2 Lumen 7fr X 150mm | 681704 | FDA UDI | Class II | Active |
| Merit Medical® | 10884450325169 | FDA UDI | Class II | Active |
| Ta3000 Angiographic Manifold | 682111 | FDA UDI | Class II | Active |
| Safedraw(tm) Ta4812sdt | 682144 | FDA UDI | Class II | Active |
| Jewish Hospital-Single Arterial Line | 686973 | FDA UDI | Class II | Active |
| 1w-Admic | 682113 | FDA UDI | Class II | Active |
| Careflow(tm) 3 Lumen 7fr X 150mm | 681721 | FDA UDI | Class II | Active |
| Careflow(tm) 2 Lumen 5fr X 60mm | 681628 | FDA UDI | Class II | Active |
| Hpt06 High Pressure Tubing 6 Inch | 682248 | FDA UDI | N/A | Active |
| Ta3101 Angiographic Manifold | 682141 | FDA UDI | Class II | Active |
| Hta3201 Angiographic Manifold | 682277 | FDA UDI | Class II | Active |
| Meritrans DTXPlus® | 10884450463854 | FDA UDI | Class II | Active |
| Sheath Intro Pop Kit 7fr L5 Mult=5/50 | 680150 | FDA UDI | Class II | Active |
| Merit Medical® | 10884450360511 | FDA UDI | Class II | Active |
| Tc-Mq-2 Dts Intfc Ca Molded Marquette | 684102 | FDA UDI | Class II | Active |
| Critiflo(tm) Ta1018 (30ml/Hr) | 682065 | FDA UDI | Class II | Active |
| Tc-Envoy Intfc 7ft Mennen Blue | 684262 | FDA UDI | Class II | Active |
| Tc-Sa Dts Intfc Ca Spacelabs W/Neg Cal | 684084 | FDA UDI | Class II | Active |
| Careflow(tm) 1 Lumen 3fr X 200mm | 681638 | FDA UDI | Class II | Active |
| Safedraw™ | 10884450326449 | FDA UDI | Class II | Active |
| Tc-Se Nly 18in Intfc Ca Siemens | 684240 | FDA UDI | Class II | Active |
| Meritrans DTXPlus® | 10884450322922 | FDA UDI | Class II | Active |
| Criticath Sp5107s Td Catheter | 680352 | FDA UDI | Class II | Active |
| Careflow(tm) 1 Lumen 7fr X 150mm | 681707 | FDA UDI | Class II | Active |
| Careflow(tm) 5 Lumen 9.5fr X 200mm | 681737 | FDA UDI | Class II | Active |
| Criticath Sp5107-14 Td Catheter | 680355 | FDA UDI | Class II | Active |
| Tc-Se/Sc6000 Dts Intfc Ca Siemens | 684178 | FDA UDI | Class II | Active |
| Merit Medical® | 00884450330838 | FDA UDI | Class II | Active |
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