Avantor Performance Materials Poland S.A.
PL-MF-000037589 · Poland · Gliwice
Avantor Performance Materials Poland S.A. is registered in the European database on medical devices as a manufacturer, with 48 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
Devices declared under this manufacturer
- CyMet 22 CN Free
- CyMet 610
- Diluid™ 22
- Diluid™ Abacus
- Diluid™ Mindray
- Diluid™ NR
- Diluid™ ST1600/2000
- Diluid™/Sheath 3200-4000
- Formaldehyde 4% - Cubitainer (Bag-in-box)
- Formaline Solution 10% V/V
- Hypochlorite Solution 0,5%
- Hypochlorite Solution 5%
Showing 12 of 48 declared devices.
Catalogue references include 3430.9020, 3483.9020PC, 3832.9020, 3933.1000MB, 3933.9010, 3936.1000.
European nomenclature codes declared: W0103010105, W01030705, W01030799, W01030706, W0103030501.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | Avantor Performance Materials Poland S.A. (PL) · FDA 3011558129 |
| Devices in EUDAMED | 48 |
| Country of registration | Poland |
Device-level evidence
| Devices with a numeric GTIN | 48 |
|---|---|
| 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. Avantor Performance Materials Poland S.A. is registered in the United States but was not found in the Canadian register.