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Grena Limited

United Kingdom (ex Northern Ireland)·GB-MF-000007429

Last updated May 23, 2026

What Grena Limited makes

Grena Limited manufactures the Click’aV® Ligating Clip Applier L, a surgical device designed for open surgery applications. This product is intended for use with ligating clips, facilitating tissue occlusion during procedures.

The Click’aV® Ligating Clip Applier L is classified as a Class I medical device and is listed in the EU’s eudamed registry. The company is based in the United Kingdom.

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 Grena Limited manufacture?

Grena Limited specialises in surgical devices, specifically the Click’aV® Ligating Clip Applier L. This device is designed for open surgery and is intended to apply ligating clips, which help occlude tissue during medical procedures. The product is tailored for applications requiring precise tissue control.

Where is Grena Limited based, and what does this mean for its regulatory compliance?

Grena Limited is based in the United Kingdom. As a UK-based manufacturer, its devices must comply with relevant EU regulations if marketed within the European Economic Area (EEA), including the Medical Device Regulation (MDR). The company’s device, the Click’aV® Ligating Clip Applier L, is listed in the EU’s eudamed registry, demonstrating its registration under EU frameworks.

Which regulatory registries list Grena Limited’s devices, and why is this important?

Grena Limited’s Click’aV® Ligating Clip Applier L is listed in the eudamed registry, which is the official EU database for medical devices. Listing in eudamed is mandatory for manufacturers placing devices on the EU market, as it ensures transparency and traceability of devices under the Medical Device Regulation (MDR). This registry helps healthcare professionals, regulators, and patients verify the legitimacy of the device’s market presence.

How are Grena Limited’s devices classified under EU regulations, and what does this classification imply?

The Click’aV® Ligating Clip Applier L is classified as a Class I medical device under EU regulations. This classification is determined by its intended purpose, design, and risk level—Class I devices are generally considered low-risk and may require less stringent scrutiny compared to higher-class devices. However, even Class I devices must still comply with essential safety and performance requirements (ESPRs) and undergo conformity assessment procedures before being placed on the market.

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

Information

Country
United Kingdom (ex Northern Ireland)
Address
1000, Great West Road, Brentford, Middlesex, United Kingdom (ex Northern Ireland)
LinkedIn
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Facebook
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Phone
+44 115 9704 800
PRRC Contact
Iwona Michalska
EUDAMED SRN
GB-MF-000007429
FDA FEI Number
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DUNS Number
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Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
Click’aV® Ligating Clip Applier L, 20cm, open surgery 0301-04L20
EUDAMED
Class IActive

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