Turnkey Cosmetic Production Line— One Supplier, Complete Line
KLM/KVM · KFM · KCM ·KTM · KM-RO · CE certified
What's Holding Your Line Back?
Batch inconsistency → KLM/KVM
Process water quality → KM-RO
Manual filling
Multi-vendor risk → Kosmix line
Four Stages. One Line
01 KM-RO — Water purification
02 KLM/KVM — Vacuum emulsification
03 KFM — Automatic filling
04 KCM + KTM — Capping & labeling
Equipment your auditors will approve.
Selling cosmetics into the EU, US, or UK means your manufacturing equipment must meet the same compliance bar as your formula. Kosmix machines are designed with regulatory requirements built in — not bolted on.
What's included in the CE documentation package
CE Declaration of Conformity, Technical Construction File, Risk Assessment, electrical and pneumatic schematics, EN 10204 3.1 material certificates for all 316L contact parts, and full Operations & Maintenance manual. IQ/OQ protocol templates provided for GMP validation.
GMP-aligned equipment design
No dead legs in pipework, mirror-polished contact surfaces (Ra ≤0.4 μm), CIP/SIP capability, and full traceability of contact-part materials — meeting ISO 22716 requirements throughout the production line.
EU Cosmetics Regulation (EC) 1223/2009
Material traceability, mirror-finish contact surfaces, and GMP-aligned documentation support Article 8 manufacturing compliance for products sold in the European market.
US FDA 21 CFR Part 700–740
IQ/OQ documentation structured to support FDA cosmetic GMP inspections. The KM-RO system produces USP Purified Water quality for process water compliance.
ISO 22716 — Good Manufacturing Practice
Equipment design, CIP capability, and documentation structure align fully with ISO 22716 — the global GMP standard for cosmetics recognised by EU, FDA, and TGA.
CE Machinery Directive 2006/42/EC
All Kosmix machines carry full CE declaration with technical file and risk assessment — legally required for installation and operation in EU, EEA, and UK markets.