HP Vitaran i (PN)
£69.00
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product description
HP Vitaran i is a Korean-manufactured polynucleotide (PN) medical device produced by BR PHARM Co., Ltd. It contains 20 mg/mL Polynucleotide Sodium and is designed specifically for professional aesthetic treatment of the delicate eye area. The product is supplied as a pre-filled syringe and is classified as a Class III medical device.
Mechanism of Action
HP Vitaran i contains Polynucleotide Sodium (PN), a biocompatible material used in aesthetic medicine to support skin regeneration and tissue remodelling. It is formulated for the delicate periorbital area, where PN treatments are intended to support skin quality, hydration and elasticity.
Key Benefits & Uses
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- Periorbital skin: Designed for professional treatment around the eye area
- Skin quality: Supports improvement in the appearance and condition of delicate skin
- Hydration: Helps support improved skin hydration
- Elasticity: Used as part of aesthetic protocols intended to improve skin elasticity and firmness
- Fine lines: Designed for use around the eye area where fine lines and skin laxity may be concerns
- Active ingredient: Polynucleotide Sodium
- Concentration: 20 mg/mL
- Product type: Polynucleotide medical device
- Classification: Class III medical device
- Packaging: 1 × 1 mL pre-filled syringe
- Intended treatment area: Periorbital / eye area
- Needle specification: 34G × 4 mm
- Shelf life: 36 months from the date of manufacture
- Manufactured by BR PHARM Co., Ltd. in South Korea
- Contains 20 mg/mL Polynucleotide Sodium
- Specifically designed for the delicate eye area
- Supplied in a convenient pre-filled syringe
- Class III medical device
- 36-month shelf life from the date of manufacture
| Question | Answer |
| What is HP Vitaran i? | A polynucleotide (PN) medical device manufactured by BR PHARM for professional aesthetic use around the eye area. |
| What is the active ingredient? | Polynucleotide Sodium. |
| What is the concentration? | 20 mg/mL. |
| How is it supplied? | 1 × 1 mL pre-filled syringe. |
| What area is it designed for? | The periorbital / eye area. |
| What needle is specified? | 34G × 4 mm. |
| What is its shelf life? | 36 months from the date of manufacture. |
| Who should administer it? | A qualified medical professional in accordance with the official Instructions for Use and local regulations. |
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