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"Wenley Asia Pacific" Delmar inspection gloves - Taiwan Registration 52cf5bf0719fb463c66f60877bd0d39c

Access comprehensive regulatory information for "Wenley Asia Pacific" Delmar inspection gloves in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 52cf5bf0719fb463c66f60877bd0d39c and manufactured by PT. WRP BUANA MULTICOPORA. 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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52cf5bf0719fb463c66f60877bd0d39c
Registration Details
Taiwan FDA Registration: 52cf5bf0719fb463c66f60877bd0d39c
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Device Details

"Wenley Asia Pacific" Delmar inspection gloves
TW: โ€œๆบซๅˆฉไบžๅคชโ€ๅพท็‘ชๆชข้ฉ—ๆ‰‹ๅฅ—
Risk Class 1
Cancelled

Registration Details

52cf5bf0719fb463c66f60877bd0d39c

DHA04400098804

Company Information

Indonesia

Product Details

Patient examination gloves are disposable equipment used to prevent contamination between the patient and the examiner based on medical necessity and are placed on the examiner's hands or fingers.

J General hospital and personal use equipment

Dates and Status

Oct 18, 2005

Oct 18, 2010

Oct 11, 2010

Cancellation Information

Logged out

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