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Sign in to claim this brandMETRIX COMPANY, THE
US
Last updated May 24, 2026
What METRIX COMPANY, THE makes
The company manufactures intravenous administration bags and bottles, as well as medication transfer sets designed for hospital and clinical use. The SECURE® line includes products for secure drug administration, while the CORMIX line focuses on mixing and transferring medications in controlled environments.
All products fall under FDA Class II regulation and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States, adhering to applicable U.S. medical device compliance requirements.
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 Metrix Company manufacture?
Metrix Company specializes in intravenous administration devices, including bags and bottles for fluid delivery, as well as medication transfer sets. Their product lines include the SECURE® series, designed for secure drug administration, and the CORMIX series, which focuses on controlled mixing and transferring of medications in clinical settings.
Where is Metrix Company based?
Metrix Company is headquartered in the United States. Their operations and manufacturing are conducted within the country, ensuring compliance with U.S. medical device regulations.
Which regulatory registries list Metrix Company’s devices?
Metrix Company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify their Class II medical devices, including intravenous administration bags, bottles, and medication transfer sets.
How are Metrix Company’s devices classified by the FDA?
All of Metrix Company’s devices fall under FDA Class II classification. This classification applies to products that generally pose moderate risk and require special controls to ensure safety and effectiveness, such as their SECURE® and CORMIX product lines.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- vescomedical.com
- —
- —
- [email protected]
- Phone
- 6149145991
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 043046283
Catalogue (67)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Secure® | 66055 | FDA UDI | Class II | Active |
| Secure® | 66100 | FDA UDI | Class II | Active |
| Cormix | MS64055 | FDA UDI | Class II | Unknown |
| Secure® | 66125 | FDA UDI | Class II | Active |
| Secure® | 66110 | FDA UDI | Class II | Active |
| Secure® | 66041 | FDA UDI | Class II | Active |
| Secure® | 58719 | FDA UDI | Class II | Active |
| Secure® | 66040 | FDA UDI | Class II | Active |
| Cormix | MS64205 | FDA UDI | Class II | Active |
| Secure® | 66653 | FDA UDI | Class II | Active |
| Cormix | MS64783 | FDA UDI | Class II | Unknown |
| Secure® | 66615 | FDA UDI | Class II | Active |
| Secure® | 66651 | FDA UDI | Class II | Active |
| Cormix | MS64235 | FDA UDI | Class II | Unknown |
| Cormix | MS64215 | FDA UDI | Class II | Active |
| Cormix | MS64125 | FDA UDI | Class II | Active |
| Secure® | 66042 | FDA UDI | Class II | Active |
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