Visco-Elastic Intradermal Implant according to TU 32.50.50-004-03127020-2020

Available versions of the visco-elastic intradermal implant:

1. VISCOLINE® HYDRO

Syringe, 1.0 ml – produced by SCHOTT Swiss AG, Switzerland (RU № FSZ 2009/04195), or Becton Dickinson France S.A.S., France (RU № FSZ 2011/11237), or Shandong Weigao Group Medical Polymer Company Limited, China (RU № RZN 2013/764) – 1 pc
Needle 30G 1/2" – produced by R.I.MOS. S.r.l., Italy (RU № FSZ 2011/09452), or BIOTEKNE S.R.L., Italy (RU № FSZ 2011/10175), or Becton Dickinson Medical (S) Pte Ltd., Singapore (RU № FSZ 2008/03143), or TERUMO Europe N.V., Belgium (RU № RZN 2018/7086), or TSK Laboratory, Japan (RU № FSZ 2011/10609) – 2 pcs
Instruction – 1 pc
Label – 2 pcs

2. VISCOLINE® BASIC

Syringe, 1.0 ml – same manufacturers as above – 1 pc
Needle 27G 1/2" – same manufacturers as above – 2 pcs
Instruction – 1 pc
Label – 2 pcs

3. VISCOLINE® LIPS

Syringe, 1.0 ml – same manufacturers as above – 1 pc
Needle 27G 1/2" – same manufacturers as above – 2 pcs
Instruction – 1 pc
Label – 2 pcs

4. VISCOLINE® INTENSE

Syringe, 1.0 ml – same manufacturers as above – 1 pc
Needle 27G 1/2" – same manufacturers as above – 2 pcs
Instruction – 1 pc
Label – 2 pcs

If your organization wants to sell medical equipment, medical products or medical consumables in Russia, for example, Visco-Elastic Intradermal Implant according to TU 32.50.50-004-03127020-2020, then our information portal MEDCOMMERCE can help you with this. To do this, simply fill out the feedback form by clicking on the link FEEDBACK FORM.

The products posted on our website are approved for use in Russia by the state regulator Roszdravnadzor (Federal Service for Surveillance in Healthcare). The information is for informational purposes only.

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