Armaviskon® MN for Peritendinous and Intra-Articular Injection According to TU 32.50.50-019-64260974-2019

The product Armaviskon® MN is intended for peritendinous and intra-articular injection and complies with technical specifications TU 32.50.50-019-64260974-2019.

Kit Contents:

Armaviskon® MN solution for peritendinous and intra-articular injection – 2 ml
Syringe in sterile pouch or blister packaging (manufacturer options):
- Becton Dickinson France S.A.S., France (Registration Certificate No. FSZ 2011/11237)
- Gerresheimer Bünde GmbH, Germany (RC No. FSZ 2011/10770)
- Shandong Weigao Group Medical Polymer Co., Ltd., China (RC No. RZN 2013/764)
- Schott Schweiz AG, Switzerland (RC No. FSZ 2009/04195)
- Stevanato Group S.p.A., Italy (RC No. FSZ 2012/12068)
Quantity: 1 or 2 pcs
Needle options (varied gauge and length) from:
- Terumo Europe N.V., Belgium (RC No. RZN 2018/7086)
- HIRANA T.Injecta a.s., Slovak Republic (RC No. FSZ 2007/00712)
- Tai-Chang Industrial Co., Korea (RC No. FSZ 2011/09101)
Types include:
- 18G 1½" (1.2×40 mm)
- 21G 1½" (0.8×40 mm)
- 21G 2" (0.8×50 mm)
- 18G 2" (1.2×50 mm)
- 18G 4" (1.2×100 mm)
- 21G 4¾" (0.8×120 mm)
- 21G 4" (0.8×100 mm)
- 25G 1½" (0.5×40 mm)
- 27G 1½" (0.4×40 mm)
- 26G 1½" (0.45×40 mm)
Quantity: 1, 2, or 4 pcs (if required)
Tracking labels – 3, 6, or 12 pcs (if required)
Product label – 1 or 2 pcs
Instructions for use – 1 copy
Cardboard carton (consumer packaging) – 1 unit

If your organization wants to sell medical equipment, medical products or medical consumables in Russia, for example, Armaviskon® MN for Peritendinous and Intra-Articular Injection According to TU 32.50.50-019-64260974-2019, 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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