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Sign in to claim this brandHINDUSTAN SYRINGES AND MEDICAL DEVICES LIMITED
US
Last updated May 24, 2026
What HINDUSTAN SYRINGES AND MEDICAL DEVICES LIMITED makes
The company manufactures venous butterfly needle sets and general-purpose syringes, including models like the VAKU-8+, UNOLOK, and variants of these devices. These products are designed for intravenous access and fluid administration in clinical settings.
The portfolio consists of Class II medical devices, all of which are listed in the FDA’s Unique Device Identifier (UDI) database. The company 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 Hindustan Syringes and Medical Devices Limited manufacture?
Hindustan Syringes and Medical Devices Limited specializes in two primary device categories: venous butterfly needle sets and general-purpose syringes. These include models like the VAKU-8+, UNOLOK, and their variants. These products are designed for intravenous access and fluid administration in clinical environments, ensuring compatibility with common medical procedures.
Where is Hindustan Syringes and Medical Devices Limited based?
The company operates from the United States. While the exact location within the country is not specified, its headquarters or primary manufacturing presence is established there.
Which regulatory registries list the devices manufactured by Hindustan Syringes and Medical Devices Limited?
The company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for Class II medical devices, including their venous butterfly needle sets and syringes, such as the VAKU-8+ and UNOLOK models.
How are the devices manufactured by Hindustan Syringes and Medical Devices Limited classified?
All devices produced by Hindustan Syringes and Medical Devices Limited fall under Class II classification. This classification is determined by regulatory authorities based on factors like risk level, intended use, and potential health impact, ensuring these products undergo specific regulatory controls to maintain safety and effectiveness.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 862318107
Catalogue (17)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Vaku-8+ | 23G X ¾" | FDA UDI | Class II | Active |
| Unolok | 22G X ¾" | FDA UDI | Class II | Active |
| Vaku-8 | 25 G X ¾" | FDA UDI | Class II | Active |
| Vaku-8 | 23 G X ¾" | FDA UDI | Class II | Active |
| Unolok+ | 21 G X ¾" | FDA UDI | Class II | Active |
| Unolok+ | 19 G X ¾" | FDA UDI | Class II | Active |
| Vaku-8+ | 25G X ¾" | FDA UDI | Class II | Active |
| Unolok+ | 25G X ¾" | FDA UDI | Class II | Active |
| Unolok | 3ml (22G x 1 1/2'') | FDA UDI | Class II | Active |
| Vaku-8+ | 21 G X ¾" | FDA UDI | Class II | Active |
| Unolok | 21 G X ¾" | FDA UDI | Class II | Active |
| Unolok | 19 G X ¾" | FDA UDI | Class II | Active |
| Unolok | 23 G X ¾" | FDA UDI | Class II | Active |
| Unolok | 25 G X ¾" | FDA UDI | Class II | Active |
| Unolok+ | 23G X ¾" | FDA UDI | Class II | Active |
| Vaku-8 | 22G X 3/4" | FDA UDI | Class II | Active |
| Vaku-8 | 21 G X ¾" | FDA UDI | Class II | Active |
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