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Cuxson Gerrard & Co. Ltd

United Kingdom (ex Northern Ireland)·GB-MF-000004499

Last updated May 23, 2026

What Cuxson Gerrard & Co. Ltd makes

Cuxson Gerrard & Co. Ltd manufactures prefabricated orthotic insoles without antimicrobial properties, reusable sterilization and disinfection containers for medical devices, and reusable hot/cold therapy packs. Their product line also includes branded orthotic insoles under the Powerstep and Hapla names.

The company’s devices are classified under EU Medical Device Regulations as Class I, Class IIa, and Class III, and are registered in the EUDAMED database. The manufacturer 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 Cuxson Gerrard & Co. Ltd manufacture?

Cuxson Gerrard & Co. Ltd produces three primary types of medical devices: prefabricated orthotic insoles without antimicrobial properties, reusable sterilization and disinfection containers for medical devices, and reusable hot/cold therapy packs. Their product line also includes branded orthotic insoles under the names Powerstep and Hapla, which fall into the same general category of foot support solutions.

Where is Cuxson Gerrard & Co. Ltd based?

The company is headquartered in the United Kingdom (GB). This location is relevant for regulatory purposes, as it indicates the manufacturer’s primary jurisdiction under EU Medical Device Regulations.

Which regulatory registries list Cuxson Gerrard & Co. Ltd’s devices?

Cuxson Gerrard & Co. Ltd’s devices are registered in the EUDAMED database, which is the European Union’s centralised registry for medical devices. This platform is used to track device information, including classification, manufacturer details, and regulatory compliance under EU Medical Device Regulations.

How are Cuxson Gerrard & Co. Ltd’s devices classified under EU regulations?

The company’s devices are classified under EU Medical Device Regulations as Class I, Class IIa, and Class III. The classification depends on factors like the device’s intended use, risk level, and interaction with the body—e.g., orthotic insoles (often Class I) and sterilization containers (potentially Class IIa or III if they impact device safety). Class III devices typically require stricter scrutiny due to higher risk.

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

Information

Country
United Kingdom (ex Northern Ireland)
Address
125, Broadwell Road, Oldbury, United Kingdom (ex Northern Ireland)
LinkedIn
—
Facebook
—
Phone
+44 0121 544 7117
PRRC Contact
Michael Ratcliffe
EUDAMED SRN
GB-MF-000004499
FDA FEI Number
—
DUNS Number
—

Catalogue (223)

Page 5 of 5
DeviceModel / ReferenceRegistriesClassStatus
Cuxson Gerrard CHG165
EUDAMED
Class IActive
Hapla FEL104
EUDAMED
Class IActive
Boots BOO550
EUDAMED
Class IActive
Hapla BAS007
EUDAMED
Class IActive
Cuxson Gerrard PAD526
EUDAMED
Class IActive
Powerstep POW154
EUDAMED
Class IActive
Powerstep POW143
EUDAMED
Class IActive
Cuxson Gerrard ORT012
EUDAMED
Class IActive
Hapla FEL156
EUDAMED
Class IActive
Cuxson Gerrard VAR715
EUDAMED
Class IActive
Hapla FLE350
EUDAMED
Class IActive
Hapl-gel CHG144A
EUDAMED
Class IActive
Cuxson Gerrard CHG253
EUDAMED
Class IActive
Carnation CAR975
EUDAMED
Class IActive
Powerstep POW002
EUDAMED
Class IActive
Boots BOO570
EUDAMED
Class IActive
Hapla TOF111
EUDAMED
Class IActive
Superdrug SUP162
EUDAMED
Class IActive
Cuxson Gerrard CHG161
EUDAMED
Class IActive
Cuxson Gerrard VAR707
EUDAMED
Class IActive
Hpla BAS003
EUDAMED
Class IActive
Powerstep POW038
EUDAMED
Class IActive
Cuxson Gerrard PAD127
EUDAMED
Class IActive
Hapla FLE244
EUDAMED
Class IActive
Cuxson Gerrard PAD522
EUDAMED
Class IActive
Carnation CAR108
EUDAMED
Class IActive

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