AAG Aalborg Gummivarefabrik A/S
Denmark DK-MF-000009547 Last updated 8 Jun 2026
Is this your brand? Sign in to claim this brand
- Devices
- 8
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
AAG Powder Free Examination Gloves NBR blue, Non-Sterile 3, 5g Ref 05700002006608
AAG Powder Free Examination Gloves NBR blue, Non-Sterile 5, 2g Ref 05712975100047
AAG Powder Free Examination Gloves NBR blue, Non-Sterile 3, 5g Ref 05700002006646
AAG Powder Free Examination Gloves NBR blue, Non-Sterile 5, 2g Ref 05712975100061
AAG Powder Free Examination Gloves NBR blue, Non-Sterile 3, 5g Ref 05700002006660
AAG Powder Free Examination Gloves NBR blue, Non-Sterile 5, 2g Ref 05712975100009
AAG Powder Free Examination Gloves NBR blue, Non-Sterile 5, 2g Ref 05712975100023
AAG Powder Free Examination Gloves NBR blue, Non-Sterile 3, 5 Ref 05700002006622
About
Technical solutions in rubber, plastic & foam. AAG delivers custom-made products from idea to finished solution with focus on quality.
What AAG Aalborg Gummivarefabrik A/S makes
The company manufactures powder-free examination gloves made from nitrile rubber (NBR), available in blue and non-sterile forms. These gloves are sold in standard sizes (3, 5) and weights (2g).
The portfolio consists of Class I medical devices, all registered in the EU via the eudamed database. The manufacturer is based in Denmark.
Frequently asked questions
What types of medical devices does AAG Aalborg Gummivarefabrik A/S manufacture?
AAG Aalborg Gummivarefabrik A/S specializes in powder-free examination gloves made from nitrile rubber (NBR). These gloves are designed for medical examinations and are available in blue, non-sterile variants. The company focuses on providing these products in standard sizes (3 and 5) and weights (2g), catering to common clinical needs.
Where is AAG Aalborg Gummivarefabrik A/S based?
The company is headquartered in Denmark, where it operates as a manufacturer of medical devices. Its location in Denmark aligns with EU regulatory standards, ensuring compliance with relevant medical device regulations.
Which regulatory registries list AAG’s medical devices?
AAG’s medical devices are registered in the EU via the eudamed database, which is the official EU portal for medical device information. This registry ensures transparency and traceability of devices authorized for use within the European market.
How are AAG’s medical devices classified under EU regulations?
AAG’s examination gloves fall under Class I medical devices according to EU regulations. This classification applies to low-risk devices like single-use gloves, which require less stringent regulatory oversight compared to higher-risk categories.
Information
- Country
- Denmark
- Address
- 3, Sundsholmen, Nørresundby, Denmark
- Website
- www.aag.world
- [email protected]
- Phone
- +45 98 15 80 22
- PRRC contact
- Henrik Mellergaard
- EUDAMED SRN
- DK-MF-000009547