Devices

Restylane SubQ Lidocaine

Model / Serial
Implanted device?
Yes
Product Description
Implant
Manufacturer
Q-Med AB
1 Event
- Field Safety Notices about Restylane SubQ Lidocaine

Manufacturer

Q-Med AB

Manufacturer Parent Company (2017)
Nestlé S.A.
Source
SMPA

5 devices with a similar name

Learn more about the data here

Restylane SubQ Lidocaine- Galderma Q-Med

Model / Serial
Product Description
medical_device
Manufacturer
Galderma Q-Med

Restylane SubQ Lidocaine 2ml dermal filler

Model / Serial
Product Description
Press release: Recall of Restylane SubQ Lidocaine 2ml dermal filler
Manufacturer
Q-Med AB

Restylane SubQ Lidocaine (Used for facial tissue augmentation)

Model / Serial
Restylane SubQ Lidocaine (Used for facial tissue augmentation)Lot numbers: 11907 and 11516Article numbers: 10-77001, 107702, 10-77005ARTG number: 193814
Manufacturer
Q-Med (Sweden) Australia Pty Ltd

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

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