Meheco - Gowns - Disposable, Surgical (SMS) G-SG-EU-01
Non Technical and Terms
Inspection and testing will be performed prior to and during production along with a final random inspection of finished products by a Bank approved independent inspection agency. The inspection contract will be let by Meheco to the approved inspection agency with costs passed through to the Borrower to pay.
Some countries have an offer from Meheco on a CIP freight basis, this is stated in the ROI. Where freight is offered, Meheco will organize the delivery of goods to the agreed destination and the borrower must pay for the carriage. The estimated freight costs are on each borrower’s ROI.
Where freight costs are not stated in a Borrower’s ROI then the carriage is Free on Board (FOB). The borrower is responsible for the cost of shipping and insurance from the country of origin to the product’s final destination in their country.
Note: Regardless of the above some countries may wish to collect the products, which can be accommodated on request.
20-30 days (from date of first advance payment)
40% on order; 60% on final acceptance of product
China Meheco Corporation is a State-Owned Enterprise in China. It is an established large-scale medical distributor with a wide distribution network. It has access to many China based manufacturers with large production capacity and some stock available for faster delivery.
Contact - For technical questions or assistance determining your requirements contact: Wenhui Sun, Project Director, Meheco Corporation. Email: 孙文辉 email@example.com
Single use, woven material, length mid-calf, sterilizable. Critical zones may be more fluid resistant than non-critical zones. Reusable gowns should meet the minimum performance requirements after maximum suggested laundering cycles.
World Health Organization’s Standards:
AAMI PB70 and ASTM F2407, EN 13795, EN 13034 - Type PB  (stitched gown), with minimum hydrostatic head of 50 cmH2O, YY/T 0506 or alternative equivalent set of standards, EN 556, if sterile, or alternative equivalent set of standards. EU PPE Regulation 2016/425 and EU MDD Directive 93/42/EEC FDA Class I or II medical device, or equivalent.