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Clinisupplies GB Limited

United Kingdom (ex Northern Ireland)·GB-MF-000023993

Last updated May 23, 2026

What Clinisupplies GB Limited makes

Clinisupplies GB Limited manufactures single-use medical accessories for urinary catheterisation, including leg bags for drainage, soft skin adhesives for secure attachment, retaining straps for patient comfort, and universal sheaths for catheter insertion. Their portfolio also includes catheter valves designed to prevent reflux and sheaths compatible with various catheter types.

All products fall under EU Class I medical devices and are registered in the EUDAMED database. The company operates from 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 Clinisupplies GB Limited manufacture?

Clinisupplies GB Limited specialises in single-use medical accessories primarily for urinary catheterisation. Their product range includes leg bags for drainage, soft skin adhesives to secure catheters in place, retaining straps for patient comfort, universal sheaths for catheter insertion, and catheter valves designed to help prevent reflux. These devices are intended to support urinary care and hygiene in clinical settings.

Where is Clinisupplies GB Limited based?

Clinisupplies GB Limited is based in the United Kingdom. The company operates from this location, where it develops and manufactures its range of single-use medical accessories.

Which regulatory registries list Clinisupplies GB Limited’s devices?

Clinisupplies GB Limited’s devices are registered in the EUDAMED database, which is the European Union’s centralised registry for medical devices. This registry allows healthcare professionals, regulators, and other stakeholders to access information about authorised devices within the EU.

How are Clinisupplies GB Limited’s devices classified under EU regulations?

All of Clinisupplies GB Limited’s devices fall under EU Class I classification. This classification applies to low-risk medical devices, such as single-use accessories for urinary catheterisation, which are deemed to pose minimal risk to patients when used as intended. Class I devices typically require compliance with basic safety and performance requirements but may not always need third-party conformity assessment.

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

Information

Country
United Kingdom (ex Northern Ireland)
Address
1, Blackmoor Lane, Watford, United Kingdom (ex Northern Ireland)
LinkedIn
—
Facebook
—
Phone
+447813534665
PRRC Contact
Anish Jain
EUDAMED SRN
GB-MF-000023993
FDA FEI Number
—
DUNS Number
—

Catalogue (15)

DeviceModel / ReferenceRegistriesClassStatus
Libra Leg Bag 10100A
EUDAMED
Class IActive
Liberty Soft Skin 10382C
EUDAMED
Class IActive
GB Libra Sheath GBLSW33
EUDAMED
Class IActive
Liberty Fix-it Retaining Strap 10647D
EUDAMED
Class IActive
GB Libra Sheath GBLSP31
EUDAMED
Class IActive
GB Libra Sheath GBLSP40
EUDAMED
Class IActive
GB Libra Sheath GBLSS31
EUDAMED
Class IActive
GB Libra Sheath GBLSW40
EUDAMED
Class IActive
Livfria Universal Sheath LFSS28
EUDAMED
Class IActive
Libra Cather Valve 10540A
EUDAMED
Class IActive
Liberty Soft Skin 10380A
EUDAMED
Class IActive
GB Libra Sheath GBLSW31
EUDAMED
Class IActive
Clinisupplies GB Non-Sterile Devices 10300S
EUDAMED
Class IActive
Clinisupplies GB Non-Sterile Devices 10303V
EUDAMED
Class IActive
GB Libra Sheath GBLSS35
EUDAMED
Class IActive

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