EU → US Device Access

CellPath Ltd

GB-MF-000022744 · United Kingdom · Newtown, Powys

CellPath Ltd is registered in the European database on medical devices as a manufacturer, with 1 092 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

other1 086
Class IIa6

Most frequent device types declared: POTS & PAILS, Claritex, BIOPAD BIOPSY PAD, CELLSAFE+, Profile LBC.

Authorised representative in the Union: NL-AR-000000116.

United States market access

FDA establishment registerRegistered with FDA
Matched entryCELLPATH LTD (GB) · FDA 3005787343
Devices in EUDAMED1 092
Country of registrationUnited Kingdom

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