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Israel·IL-MF-000009312
Last updated May 30, 2026
What LAMINATE MEDICAL TECHNOLOGIES LTD makes
Laminate Medical Technologies Ltd manufactures arteriovenous fistula extraluminal mesh-sleeves and single-use open-surgery blood vessel sizers. The VasQ product line includes variants such as VasQ DMST and a model selection tool, designed for vascular access procedures. These devices are intended for use in creating or assessing blood vessels during surgical interventions.
The company’s devices are classified under EU Medical Device Regulations as Class I, Class II, and Class IIa, with listings in the EUDAMED database and the FDA’s UDI system. The manufacturer is based in Israel and adheres to regulatory requirements for these device categories.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What does LAMINATE MEDICAL TECHNOLOGIES LTD manufacture?
Laminate Medical Technologies Ltd manufactures arteriovenous fistula extraluminal mesh-sleeves and single-use open-surgery blood vessel sizers, with their primary product line being the VasQ device and its variants, including VasQ DMST and a model selection tool.
Where is LAMINATE MEDICAL TECHNOLOGIES LTD based?
Laminate Medical Technologies Ltd is based in Israel, as indicated by the country code 'IL' in the device data.
Which regulatory registries list LAMINATE MEDICAL TECHNOLOGIES LTD's devices?
The company's devices are listed in the EUDAMED database and the FDA's UDI system, as specified in the device data.
How are LAMINATE MEDICAL TECHNOLOGIES LTD's devices classified?
The company's devices are classified under EU Medical Device Regulations as Class I, Class II, and Class IIa, depending on the specific product and its intended use.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Israel
- Address
- 24, Raoul Wallenberg, Tel Aviv , Israel
- Website
- www.laminatemedical.com
- —
- —
- [email protected]
- Phone
- +972-3-6344246
- PRRC Contact
- Orit Yarden
- EUDAMED SRN
- IL-MF-000009312
- FDA FEI Number
- —
- DUNS Number
- 600196773
Catalogue (9)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| VasQ | 3 | FDA UDI | Class II | Active |
| VasQ | 6 | FDA UDI | Class II | Active |
| VasQ DMST | 5 unit pack | FDA UDI | Class I | Active |
| VasQ | 1 | FDA UDI | Class II | Active |
| VasQ DMST | 20 Unit pack | FDA UDI | Class I | Active |
| VasQ | 5 | FDA UDI | Class II | Active |
| VasQ | 4 | FDA UDI | Class II | Active |
| VasQ | 2 | FDA UDI | Class II | Active |
| VasQ Model Selection Tool | FG024 | EUDAMED | Class IIa | Active |
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