Russia Roszdravnadzor registration ФС 022б1778/4623-06

Single-use injection needles of the Luer type with a plastic head II-TZMOI of the following standard sizes: 036mm x 12mm; 05mm x 16mm; 06mm x 25mm; 06mm x 32mm; 07mm x 38mm; 08mm x 38mm; 12mm x 38mm and 15mm x 38mm.

RU: Иглы инъекционные однократного применения типа Луер с пластмассовой головкой ИИ-ТЗМОИ следующих типоразмеров: 036мм х 12мм; 05мм х 16мм; 06мм х 25мм; 06мм х 32мм; 07мм х 38мм; 08мм х 38мм; 12мм х 38мм и 15мм х 38мм.
Russia flagRussia·Unknown·OJSC Tyumen Plant of Medical Equipment and Instruments·Registered December 20, 2006·Class 2b
Device information
Device Name (English)
Single-use injection needles of the Luer type with a plastic head II-TZMOI of the following standard sizes: 036mm x 12mm; 05mm x 16mm; 06mm x 25mm; 06mm x 32mm; 07mm x 38mm; 08mm x 38mm; 12mm x 38mm and 15mm x 38mm.
Device Name (Russian)
Иглы инъекционные однократного применения типа Луер с пластмассовой головкой ИИ-ТЗМОИ следующих типоразмеров: 036мм х 12мм; 05мм х 16мм; 06мм х 25мм; 06мм х 32мм; 07мм х 38мм; 08мм х 38мм; 12мм х 38мм и 15мм х 38мм.
Device Type (English)
N/A
Device Type (Russian)
Unknown
Risk Class
Class 2b
OKPD Code
94 3220
Registration information
Registry Key
o24921
Registration Number
ФС 022б1778/4623-06
Registration Date
December 20, 2006
Validity Period
December 20, 2011
Manufacturer information
Country (English)
Russia
Country (Russian)
Россия
Legal Address (English)
625035 Tyumen 205 Respubliki Str.
Legal Address (Russian)
625035 г.Тюмень ул.Республики 205
About this record

Access comprehensive regulatory information for Single-use injection needles of the Luer type with a plastic head II-TZMOI of the following standard sizes: 036mm x 12mm; 05mm x 16mm; 06mm x 25mm; 06mm x 32mm; 07mm x 38mm; 08mm x 38mm; 12mm x 38mm and 15mm x 38mm. in the Russia medical device market through Pure Global AI's free database. This Class 2b medical device is registered under Roszdravnadzor registration number ФС 022б1778/4623-06 and manufactured by OJSC Tyumen Plant of Medical Equipment and Instruments. The device was registered on December 20, 2006.

This page provides complete registration details including device type, manufacturer information, country of origin (Russia), and regulatory compliance data from the official Russia Roszdravnadzor medical device database. Pure Global AI offers free access to Russia's complete medical device registry, helping global MedTech companies navigate Roszdravnadzor regulations efficiently.

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