Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011495193

FEI Number

3011495193

Entity Name

MANGAR INTERNATIONAL LIMITED

City/State/Country

Presteigne Powys, GB

Establishment Address

Presteigne Industrial Estate, Presteigne Powys LD82UF, GB

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Mangar International Ltd (Owner Number: 10048550)

Owner / Operator Contact Address

Presteigne Industrial Estate, Presteigne, GB-POW LD82UF, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Mangar Elk Lifting Cushion Mangar Bathing Cushion Mangar Surfer Bather Mangar Sit-U-Up Mangar Camel Lifting Cushion Mangar Archimedes Mangar Leglifter Mangar Handy Pillowlift Mangar Rhino Lifting Cushion Mangar Raiser Lifting Cushion Mangar Eagle Lifting Cushion Mangar Swift Transfer Slide

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FSA	Lift, Patient, Non-Ac-Powered	General Hospital	Class 1	880.5510	2015-01-26
FMR	Device, Transfer, Patient, Manual	General Hospital	Class 1	880.6785	2023-05-25

Official Correspondent

Jane Owens

US Agent Details

Simon Claridge Email: simon.claridge@winncare.uk Phone: (401) 4755826

Related Public Records

Same Entity

Mangar International Ltd

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0013-2018	Handicare Usa Inc	1	PRISM MEDICAL A-625, MAX. LOAD 625 lbs. 283 Kgs., Patient lift, non-A/C powered
Z-0014-2018	Handicare AB Maskinvagen	1	Carina Mobile Lifts, Models: a) Carina350EM, REF 6060011 b) Carina350EML, REF 60600012 c) Carina350EE, REF 60600009

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011495193. Last updated year: 2026. Please use registration number 3011495193 when referencing this establishment in official correspondence.