SunekosĀ® 1200 is an injectable preparation with anti-ageing, nourishing and firming action. Intended for older patients, it counteracts loss of facial volume, reduces deep wrinkles and hydrates. The patent-protected formula contains hyaluronic acid and a combination of amino acids, precursors of collagen and elastin. This combination helps stimulate regeneration of the extracellular matrix. SunekosĀ® 1200 is a class III medical device, available in both a needle and a cannula version. It works very well in the delicate eye area.
Recommended SunekosĀ® treatment cycle
Injection with SunekosĀ® 1200
On the same day or within 2 days, injection with SunekosĀ® 200
Break of 7 to 10 days
Injection with SunekosĀ® 200
Break of 7 to 10 days
Injection with SunekosĀ® 200
Break of 7 to 10 days
Injection with SunekosĀ® 200
Continue the treatment cycle after 4 and 7 months (injection with SunekosĀ® 1200, then on the same day or within 2 days injection with SunekosĀ® 200)
Duration of effect
over 6 months
Protocol
needle size: 27 to 30G, 13 mm
cannula size: 25 to 27 to 30G, 40 mm
injection: deep layers of the dermis
Product leaflet
The product may be used by professionals only.
Full ingredients (INCI)Non-cross-linked hyaluronic acid 30 mg/3 ml with a molecular weight of 1200 kD Amino acids:Glycine: an amino acid that activates collagen synthesisL-valine: an amino acid supporting repair processesL-alanine and L-leucine: ingredients with strong antioxidant actionL-lysine: an ingredient that strengthens skin resistanceL-proline: strong hygroscopic properties Glycine: an amino acid that activates collagen synthesis L-valine: an amino acid supporting repair processes L-alanine and L-leucine: ingredients with strong antioxidant action L-lysine: an ingredient that strengthens skin resistance L-proline: strong hygroscopic properties
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Nothing on this page is clinical, medical or training advice. Which product to use, on whom, in what quantity and by what technique are decisions for a qualified practitioner working within their own scope of practice, insurance and professional obligations.
Professional use
Where a manufacturer states that a product is for professional use only, that is how we supply it. We may ask you to evidence your professional registration before we sell you a restricted product, and we keep a record that we checked.
CE marking
Where a product is a medical device, it carries the CE marking applied by its manufacturer under the relevant EU regulation. CE marking means the manufacturer has declared conformity with the applicable requirements. It is not an approval or an endorsement by us, and we describe products as CE marked, never as CE approved.
Instructions, batches and certificates
Always read the manufacturer instructions for use supplied with the product. Where you need a declaration of conformity, a batch number, an expiry date or a certificate, ask us and we will get it.
If something goes wrong
A product safety or quality concern is urgent and is handled differently to an ordinary complaint. Stop using the product, keep the packaging and the batch number, and tell us the same day. Full detail is in our complaints and product safety policy.
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