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GENMED ENTERPRISES INTERNATIONAL LTD

United Kingdom GB-MF-000010687 Last updated 23 May 2026

Devices
180
Registries
EUDAMED
FDA recalls
0

Catalogue180

Page 1 of 4

Showing 1-50 of 180

EUDAMED certificates1

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

EUDAMED certificates (1)

TÜV Rheinland LGA Products GmbH 0197 1 certificate

  • DZ 2318749-1 Supplemented Expires in 86 days

    Quality assurance EU MDR

    Issued
    29 Aug 2025
    Expires
    20 Jan 2027
    Reason
    Change approved

Authorised representatives

What GENMED ENTERPRISES INTERNATIONAL LTD makes

GenMed Enterprises International Ltd manufactures single-use surgical instruments, including sterile trocars, wound protectors, suction irrigation devices, and specimen retrieval bags. These products are designed for minimally invasive procedures and are intended for one-time clinical use to reduce infection risk and cross-contamination.

The company’s portfolio is classified under EU Medical Device Regulation (MDR) as Class IIa devices and is registered in the EUDAMED database. The products are listed for commercialisation within the European Economic Area.

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 GenMed Enterprises International Ltd manufacture?

GenMed Enterprises International Ltd specialises in single-use surgical instruments. Their portfolio includes sterile trocars, sterile wound protectors, sterile suction irrigation devices, and sterile specimen retrieval bags. These devices are designed for minimally invasive surgical procedures and are intended for one-time clinical use to minimise infection risks and cross-contamination.

Where is GenMed Enterprises International Ltd based?

GenMed Enterprises International Ltd is based in the United Kingdom (GB). The company’s headquarters and operations are located within this region.

Which regulatory registries list GenMed Enterprises International Ltd’s devices?

GenMed Enterprises International Ltd’s devices are listed in the EUDAMED database, which is the European Union’s medical device registry. This registration reflects their compliance and commercialisation status within the European Economic Area.

How are GenMed Enterprises International Ltd’s devices classified under EU regulations?

GenMed Enterprises International Ltd’s devices fall under the classification of Class IIa medical devices according to the EU Medical Device Regulation (MDR). This classification is determined based on factors like the intended use, risk associated with the device, and its potential impact on patient safety, ensuring appropriate regulatory oversight.

Are GenMed Enterprises International Ltd’s devices intended for reuse?

No, GenMed Enterprises International Ltd’s devices are explicitly designed for single-use only. This design choice helps reduce the risk of infection and cross-contamination in clinical settings, aligning with best practices for surgical instrument safety.

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

Information

Country
United Kingdom(from SRN)
Address
Fountain House, Fountain Lane, St Mellons, Cadiff, United Kingdom (ex Northern Ireland)
Phone
0044 (0)7532708528
PRRC contact
Yan Li
EUDAMED SRN
GB-MF-000010687