Виво Медикал Технолоджис
Company-provided description, not an official-source fact. Certifications, capacities, years and market positions stated in it are the company's own claims until a record below confirms them.
SteriPak Service réalise des prototypes de dispositifs médicaux, des petites séries de dispositifs médicaux, réalise une...
SteriPak Service produit des prototypes de dispositifs médicaux, de petites séries de dispositifs médicaux, réalise un cycle complet de développement d'emballages, à la fois primaires et de consommation, et après avoir reçu des matières premières ou des composants en entrée, produit une petite série à part entière, comprenant un ensemble complet d'accessoires...
- Type
- Not established by any record (our catalog import lists it as manufacturer; that is not evidence of the role)
- Role
- Role not established by any record
- Location
- Russia
- Website
- vivoline.su
- Categories
- Emballage et fournitures d'impression, Fournitures médicales et de santé, Pièces et accessoires auto
- Markets
- Russie
What is established and what is not
No researcher review has been written for this company yet. No fact of any kind is on file either. Nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)
- Upcoming, not yet applicable on 2026-10-15: If the goods are paper, board or printed products, placing them on the EU market falls under the Deforestation Regulation (EUDR) due-diligence regime; packaging machinery itself does not. The EU Deforestation Regulation applies to large and medium operators from 30 December 2026 and to micro and small operators from 30 June 2027; due-diligence intensity depends on the risk level the Commission assigns to the country of production. European Commission (EUDR)
Goods family established: Emballage et fournitures d'impression (the company's own text), Fournitures médicales et de santé (the company's own text). The exact product, operation and trade route needed to determine a product-specific requirement are not established here. Product-specific import rules not established for the catalog category Pièces et accessoires auto: no record or company text names goods of this kind. A catalog category alone is our classification, not proof of what the company makes or sells.
Check independently
Before a first order, ask for the legal entity's registration number and country, then check it in the official register.