With the rise of the "self-pleasure economy," the personal lubricant market has seen explosive growth. However, beneath the prosperous surface, the industry has long suffered from ambiguous standards and inconsistent quality. Many consumers often only focus on price or fragrance when purchasing, neglecting the most important attribute: safety. In fact, as a product used intimately within the human body, its safety level should inherently be aligned with medical devices. Only by establishing a "medical-grade" high standard can consumer concerns truly be alleviated and the healthy development of the industry be promoted.
"Medical-grade" is not a marketing gimmick; it represents a rigorous quality management system. It requires manufacturing enterprises to meet medical device production conditions in terms of hardware facilities, such as being equipped with dust-free purification workshops and purified water systems. In terms of software management, a full-process traceability mechanism must be established, with every step from raw material procurement records to production batch records fully documented. Compared to ordinary daily chemical standards, medical-grade standards have more stringent requirements for raw material biocompatibility, allergenicity, and cytotoxicity. This is not only to meet regulatory compliance but also to ensure user safety even in extreme circumstances.
When the market returns to rationality, quality will become the ultimate barrier to brand competition. For brands, choosing an OEM factory that can provide medical-grade endorsement means equipping their products with a robust armor. This not only effectively mitigates market regulatory risks but also establishes a professional brand image in the minds of consumers through high-standard quality commitments. In future market competition, only products that dare to promise "medical-grade safety" will truly win user trust and repurchase.
PINGCHUANG Medical redefines safety standards with its global compliance certification system, possessing Class II medical device registration certificates for medical lubricating jelly, ISO13485, and US FDA, EU CE certifications. Clients do not need to invest millions or endure lengthy certification cycles; they can share our full qualification endorsements, achieving a "zero-threshold" compliant product launch, safeguarding your brand's reputation with medical-grade quality.
