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"Wenli Asia Pacific" Delmar Inspection Gloves (Powder-free) (Unsterilized) - Taiwan Registration 55fc033e1d0277f296dc59b9496845b3

Access comprehensive regulatory information for "Wenli Asia Pacific" Delmar Inspection Gloves (Powder-free) (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 55fc033e1d0277f296dc59b9496845b3 and manufactured by WRP ASIA PACIFIC SDN BHD. The authorized representative in Taiwan is SANSOME TRADING CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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55fc033e1d0277f296dc59b9496845b3
Registration Details
Taiwan FDA Registration: 55fc033e1d0277f296dc59b9496845b3
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Device Details

"Wenli Asia Pacific" Delmar Inspection Gloves (Powder-free) (Unsterilized)
TW: "ๆบซๅˆฉไบžๅคช" ๅพท็‘ชๆชข้ฉ—ๆ‰‹ๅฅ— (็„ก็ฒ‰)(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

55fc033e1d0277f296dc59b9496845b3

DHA04400913601

Company Information

Malaysia

Product Details

Limited to the first level of identification scope of the Measures for the Classification and Grading of Medical Equipment "Gloves for Patient Examination (J.6250)".

J General hospital and personal use equipment

J.6250 ็—…ๆ‚ฃๆชขๆŸฅ็”จๆ‰‹ๅฅ—

Input;; QMS/QSD

Dates and Status

Aug 26, 2010

Aug 26, 2025