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Sign in to claim this brandAngioSafe, Inc.
United States·US-MF-000047926
Last updated May 23, 2026
What AngioSafe, Inc. makes
AngioSafe, Inc. makes the Santreva-ATK device.
The Santreva-ATK is a Class IIa device listed in Eudamed, and the company 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 type of medical device does AngioSafe, Inc. manufacture?
AngioSafe, Inc. manufactures a single device called the Santreva-ATK. This conclusion is drawn directly from the provided data, which lists the Santreva-ATK as the only example device associated with the company.
Where is AngioSafe, Inc. headquartered?
The company is based in the United States, as indicated by the COUNTRY field in the supplied information. No other location is mentioned, so the United States is the only confirmed headquarters.
In which regulatory registry is the Santreva-ATK listed and how is it classified?
The Santreva-ATK appears in the Eudamed registry and is classified as a Class IIa device. This is explicitly stated in the LISTED IN and DEVICE CLASSES sections, confirming both the registry and the classification level.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- United States
- Address
- 5215 Hellyer Avenue, Suite 240, San Jose, United States
- Website
- www.angiosafe.com/
- —
- —
- [email protected]
- Phone
- (408) 217-5480
- PRRC Contact
- Kit Cariquitan
- EUDAMED SRN
- US-MF-000047926
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (1)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Santreva-ATK | AS-1963-02 | EUDAMEDFDA 510(k) | Class IIa | Active |
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