AAG Aalborg Gummivarefabrik A/S
DK-MF-000009547 · Denmark · Nørresundby
AAG Aalborg Gummivarefabrik A/S is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 9 |
|---|
Most frequent device types declared: AAG Powder Free Examination Gloves NBR blue, Non-Sterile 3,5.
Devices declared under this manufacturer
- AAG Powder Free Examination Gloves NBR blue, Non-Sterile 3,5
- AAG Powder Free Examination Gloves NBR blue, Non-Sterile 3,5g
- AAG Powder Free Examination Gloves NBR blue, Non-Sterile 5,2g
Catalogue references include 05700002006608, 05700002006622, 05700002006646, 05700002006660, 05712975100023, 05712975100047.
European nomenclature codes declared: T01020204.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| Country of registration | Denmark |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 9 |
|---|---|
| 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: Neither register. AAG Aalborg Gummivarefabrik A/S was not found in either the U.S. or the Canadian register.