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Sign in to claim this brandMEUS SRL
US
Last updated May 27, 2026
What MEUS SRL makes
MEUS SRL manufactures non-fixed blood collection needles designed for venipuncture procedures. These devices are intended for use in collecting blood samples for laboratory testing or diagnostic purposes.
The company’s products fall under FDA Class II devices and are listed in the FDA’s Unique Device Identification (UDI) system. MEUS SRL 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 MEUS SRL manufacture?
MEUS SRL specializes in manufacturing non-fixed blood collection needles, which are primarily used for venipuncture to draw blood samples for laboratory analysis or diagnostic testing. These devices are designed to facilitate safe and efficient blood collection in clinical settings.
Where is MEUS SRL based?
MEUS SRL is headquartered in the United States. The company’s location ensures compliance with U.S. regulatory standards for medical devices, including those governed by the FDA.
Which regulatory registries list MEUS SRL’s devices?
MEUS SRL’s devices are included in the FDA’s Unique Device Identification (UDI) system, which is a standardized database for tracking medical devices in the U.S. This registry helps ensure traceability and regulatory oversight of their products.
How are MEUS SRL’s devices classified under FDA regulations?
MEUS SRL’s blood collection needles fall under FDA Class II device classification. This classification is assigned based on risk assessment—Class II devices require special controls beyond general controls to ensure safety and effectiveness, such as performance standards or post-market surveillance.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- vacutestkima.it
- —
- —
- [email protected]
- Phone
- +390499719511
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 514346550
Catalogue (16)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Vacutest Kima S.r.l. | 15565 | FDA UDI | Class II | Active |
| Vacutest Kima S.r.l. | 15176 | FDA UDI | Class II | Active |
| Vacutest Kima S.r.l. | 1526506 | FDA UDI | Class II | Active |
| Vacutest Kima S.r.l. | 1526504 | FDA UDI | Class II | Active |
| Vacutest Kima S.r.l. | 15521 | FDA UDI | Class II | Active |
| Vacutest Kima S.r.l. | 15225 | FDA UDI | Class II | Active |
| Vacutest Kima S.r.l. | 1526502 | FDA UDI | Class II | Active |
| Vacutest Kima S.r.l. | 15567 | FDA UDI | Class II | Active |
| Vacutest Kima S.r.l. | 15213 | FDA UDI | Class II | Active |
| Vacutest Kima S.r.l. | 15193 | FDA UDI | Class II | Active |
| Vacutest Kima S.r.l. | 15566 | FDA UDI | Class II | Active |
| Vacutest Kima S.r.l. | 15164 | FDA UDI | Class II | Active |
| Vacutest Kima S.r.l. | 15522 | FDA UDI | Class II | Active |
| Vacutest Kima S.r.l. | 15520 | FDA UDI | Class II | Active |
| Vacutest Kima S.r.l. | 15181 | FDA UDI | Class II | Active |
| Vacutest Kima S.r.l. | 15201 | FDA UDI | Class II | Active |
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