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APA Parafricta Ltd

United Kingdom (ex Northern Ireland)·GB-MF-000006298

Last updated May 23, 2026

What APA Parafricta Ltd makes

APA Parafricta Ltd manufactures assistive crawler/mobility boards designed to aid individuals with limited mobility, enabling independent movement and support during transfers or ambulation.

The company’s products are classified as Class I medical devices and are registered in the EU’s 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 APA Parafricta Ltd manufacture?

APA Parafricta Ltd specialises in assistive crawler/mobility boards. These devices are designed to help individuals with limited mobility move independently or receive support during transfers and ambulation. The company’s focus is on products that enhance mobility and accessibility for users who may struggle with traditional walking aids.

Where is APA Parafricta Ltd based?

APA Parafricta Ltd is based in the United Kingdom. The company’s location in the UK influences its regulatory compliance, particularly for devices marketed within Europe, though this does not imply any approval status for the company itself.

Which regulatory registries list APA Parafricta Ltd’s devices?

APA Parafricta Ltd’s devices are listed in the eudamed database, which is the EU’s centralised registry for medical devices. This registry is used to track devices that have undergone the necessary conformity assessment procedures under EU regulations, such as CE marking for Class I devices.

How are APA Parafricta Ltd’s devices classified under medical device regulations?

APA Parafricta Ltd’s assistive crawler/mobility boards fall under Class I classification in the EU’s medical device regulatory framework. This classification is typically assigned to low-risk devices that pose minimal risk to users, such as certain mobility aids. Classification determines the regulatory pathway and documentation requirements for market placement.

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

Information

Country
United Kingdom (ex Northern Ireland)
Address
30, Upper High Street , Thame, United Kingdom (ex Northern Ireland)
LinkedIn
—
Facebook
—
Phone
+441869226566
PRRC Contact
Nicholas Garner
EUDAMED SRN
GB-MF-000006298
FDA FEI Number
—
DUNS Number
—

Catalogue (18)

DeviceModel / ReferenceRegistriesClassStatus
Parafricta PFFNBN-001
EUDAMED
Class IActive
Parafricta PFFB-004L
EUDAMED
Class IActive
Parafricta PFFUG-003M
EUDAMED
Class IActive
Parafricta PFFUG-001XL
EUDAMED
Class IActive
Parafricta PFFSS-003
EUDAMED
Class IActive
Parafricta PFFUG-001M
EUDAMED
Class IActive
Parafricta PFFSS-001
EUDAMED
Class IActive
Parafricta PFFB-001M
EUDAMED
Class IActive
Parafricta PFFSS-002
EUDAMED
Class IActive
Parafricta PFFUG-003XXL
EUDAMED
Class IActive
Parafricta PFFUG-001XS
EUDAMED
Class IActive
Parafricta PFFUG-003XS
EUDAMED
Class IActive
Parafricta PFFUG-002XS
EUDAMED
Class IActive
Parafricta PFFDS-001
EUDAMED
Class IActive
Parafricta PFFB-001XL
EUDAMED
Class IActive
Parafricta PFFB-004M
EUDAMED
Class IActive
Parafricta PFFUG-003XL
EUDAMED
Class IActive
Parafricta PFFUG-002S
EUDAMED
Class IActive

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