S And S Industries

Quality Compliance

S & S INDUSTRIESPLOT NO. 1111, GIDC, VITTHAL UDHYOG NAGAR – 388121,DIST: ANAND, GUJARAT, INDIA.DESIGN, MANUFACTURE, SERVICE AND SUPPLY OF LABORATORY ANDPRODUCTION EQUIPMENT FOR DYES, PIGMENTS, INKS, PHARMACEUTICALSAND AGROCHEMICALS INDUSTRIES.IAF CODE : 19,18Certificate No:26UQAK05Initial Registration Date:23/01/2026Issuance Date:23/01/2026Date of Expiry:22/01/20291st Surv. Due:23/12/20262nd Surv. Due:23/12/2027(Scan to Verify

Quality Standards

Certificate of ComplianceWe hereby declare that the technical file of product complied with the requirement ofMedical Device Regulation (MDR) 2017/745.Manufacturer:Name : S AND S INDUSTRIESAddress: PLOT NO 1111, G I D C, PHASE IV, VITHAL UDYOGNAGAR,ANAND, GUJARAT, 388121, INDIAProduct: LABORATORY PRESS, HIGH SPEED STIRRER, PLANETARY BALL MILL FOR LABORATORY, LABORATORY STIRRER, HYDRAULIC PRESS BRAKE MACHINE, BALL MILL FOR LABORATORY, SHAKER INCUBATOR, DOUBLE ACTION HYDRAULIC PRESS, VIBRO SUPER SHAKER, AUTO FILM APPLICATOR, BEAD MILL, LAB STIRRER, AUTOMATIC PIGMENT MULLERThe certification body has performed an audit of the above product quality system covering the design, manufacture and finalInspection of certified product. The quality system has been assessed, approved and is subject to continuous surveillanceaccording Medical Device Regulation (MDR) 2017/745.This certificate issued under the following conditions:1. It applies only to the quality system maintained in the manufacturing of above referenced models and it does not substitute the design or type examination procedures, if requested2. The certificate remains valid until the manufacturing conditions or the quality system are changed3. The certificate validity is conditioned by positive results of surveillance audits4. After fulfilling relevant EEC legislation, the manufacturer shall affix to each device, of the referenced models The CE mark as shown below can be used under the responsibility of the manufacturer after completion of an EEC Declaration of conformity and compliance with all relevant EEC Directives. The statement is based on a single evaluation of one sample of above mentioned product. Not imply an assessment of the whole production.:: Certificate No :: CE/26M01956Date of initial registration:First Surveillance Audit on or before: Second Surveillance Audit on or before: Re-certification Due:06 April 202605 April 202705 April 202805 April 2029This Certificate is property of MQA and remains valid Subject to satisfactory surveillance audits