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
| Class IIa | 6 |
|---|
Most frequent device types declared: BIOPAD BIOPSY PAD, CELLSAFE+, Claritex, GP, HIST/NCB-0600-11A.
Authorised representative in the Union: Emergo Europe B.V..
Devices declared under this manufacturer
- BIOPAD BIOPSY PAD - GREEN
- CELLSAFE I BIOPSY CASSETTE - WHITE LASER (THREADED)
- CELLSTOR POT CH MOUSC - 60ml - 10% NEUTRAL BUFFERED FORMALIN
- EOSIN Y STAIN 1% (ALCOHOLIC) - 1L
- Pathflow PiSmart Laser Cassettes Micro Biopsy Peach
- SYSTEM II HEX - CASSETTE - GREEN (LOOSE)
- SYSTEM II+ 2 WELL CASSETTE - ORANGE (HOPPERED)
- SYSTEM II+ 2 WELL CASSETTE - TAN (HOPPERED)
- SYSTEM II+ BIOPSY CASSETTE - TAN (HOPPERED)
- SYSTEM II+ ROUND CASSETTE - BLUE LASER (THREADED)
- SYSTEM II+ ROUND CASSETTE - WHITE (LOOSE)
- SYSTEM II+ SLOTTED CASSETTE - GREY (LOOSE)
Showing 12 of 1 092 declared devices.
Catalogue references include EAD-0104-03A, EAI-0411-10A, EAM-0505-03A, EAM-0612-05H, EAM-0802-03A, EAM-1308-72B.
European nomenclature codes declared: W0202050385, W01030708, W01030705, W01030706, W0599, W02029085.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | CELLPATH LTD (GB) · FDA 3005787343 |
| Devices in EUDAMED | 1 092 |
| Country of registration | United Kingdom |
Device-level evidence
| Devices with a numeric GTIN | 1 092 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: United States only. CellPath Ltd is registered in the United States but was not found in the Canadian register.