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Nihal Healthcare

India·IN-MF-000020686

Last updated May 23, 2026

What Nihal Healthcare makes

Nihal Healthcare manufactures sterile hypodermic syringes with needles, including a 1 ml/cc model with a 23-gauge needle packaged in ribbon form. These products are designed for single-use medical injections and are supplied in sterile, pre-filled configurations to ensure aseptic administration.

The company’s devices fall under EU medical device classifications, including Class I and Class IIa, and are registered in the EU’s eudamed database. The portfolio is regulated under European Union medical device legislation, ensuring compliance with safety and performance standards for sterile injection equipment.

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 Nihal Healthcare manufacture?

Nihal Healthcare specializes in sterile hypodermic syringes with needles, including a 1 ml/cc model with a 23-gauge needle packaged in ribbon form. These devices are designed for single-use medical injections and are supplied in sterile, pre-filled configurations to ensure safe and aseptic administration.

Where is Nihal Healthcare based?

Nihal Healthcare is based in India, as indicated by its country designation. The company’s operations and manufacturing are conducted within this region.

Which regulatory registries list Nihal Healthcare’s devices?

Nihal Healthcare’s devices are listed in the eudamed database, which is the European Union’s central registry for medical devices. This registration ensures transparency and compliance with EU medical device regulations for its products.

How are Nihal Healthcare’s devices classified under EU regulations?

Nihal Healthcare’s devices fall under Class I and Class IIa classifications in the EU. These classifications are determined based on risk levels and regulatory requirements for sterile injection equipment, ensuring appropriate oversight and compliance with safety standards.

Are Nihal Healthcare’s devices regulated under specific EU medical device legislation?

Yes, the company’s devices are regulated under the European Union medical device legislation, which governs the safety, performance, and compliance of sterile injection equipment. This framework ensures that products like hypodermic syringes meet strict regulatory criteria before being placed on the market.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
India
Address
Plot No.33, EPIP Phase-I, Jharmajri, Tehsil Baddi, Solan, Himachal Pradesh, 173205, India, Baddi, India
LinkedIn
—
Facebook
—
Phone
+91 1 795 27 12 36/37
PRRC Contact
Pawan Sharma
EUDAMED SRN
IN-MF-000020686
FDA FEI Number
—
DUNS Number
—

Catalogue (9)

DeviceModel / ReferenceRegistriesClassStatus
Nihal 8906085430133
EUDAMED
Class IActive
Nihal 8906085430157
EUDAMED
Class IActive
Sterile Hypodermic Syringe with Needle 1 ml/cc with 23G Ribbon Pack 08906085430003
EUDAMED
Class IIaActive
Nihal 8906085430119
EUDAMED
Class IActive
Nihal 8906085430164
EUDAMED
Class IActive
Nihal 8906085430140
EUDAMED
Class IActive
Nihal 8906085430171
EUDAMED
Class IActive
Nihal 8906085430126
EUDAMED
Class IActive
Nihal 8906085430102
EUDAMED
Class IActive

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