Question 1

Which quality certifications does Sterimed hold for medical disposables?

Accepted Answer

Sterimed manufacturing units operate under ISO 9001 and ISO 13485 quality management systems, hold WHO-GMP certification and CE marking for applicable device families. Batch-wise documentation, biocompatibility data and sterilisation validation reports are available to importers and distributors for regulatory dossiers.

Question 2

What sterilisation methods are used for Sterimed Foley catheters and endotracheal tubes?

Accepted Answer

Single-use urology and airway devices are terminally sterilised by Ethylene Oxide (EO) with validated cycles and routine residual testing. Each pouch carries a sterilisation indicator, lot number and expiry date so hospital storekeepers can verify traceability at the point of use.

Question 3

Does Sterimed offer OEM and private-label manufacturing for international distributors?

Accepted Answer

Yes. Sterimed supports OEM and private-label programmes including customised printing, multilingual IFUs, country-specific labelling, export cartons and shelf-ready packaging configurations for distributors in Europe, Latin America, Africa, the Middle East and Asia.

Question 4

How can overseas buyers request product catalogues and technical documentation?

Accepted Answer

International buyers can download the latest catalogue from the Downloads section or write to exports@www.citecmedical.com for size charts, material specifications, free-sale certificates and CE documentation relevant to their market.

Question 5

Which Foley catheter sizes and variants are manufactured by Sterimed?

Accepted Answer

Sterimed manufactures 2-way and 3-way latex Foley balloon catheters in Fr. 6 to Fr. 30 sizes, including high-flow, paediatric, silicone-coated and hydrophilic polymer-coated variants with 5 ml to 30 ml balloon capacities.