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"Sterry" Manual Gastroenterology-Urology Surgical Instruments and Their Accessories (Sterilization) - Taiwan Registration 38ef89c2d9f28d32ce97ad76a81764a8

Access comprehensive regulatory information for "Sterry" Manual Gastroenterology-Urology Surgical Instruments and Their Accessories (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 38ef89c2d9f28d32ce97ad76a81764a8 and manufactured by UNITED STATES ENDOSCOPY GROUP, INC.;; STERIS Corporation. The authorized representative in Taiwan is Sterry Taiwan Corporation.

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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38ef89c2d9f28d32ce97ad76a81764a8
Registration Details
Taiwan FDA Registration: 38ef89c2d9f28d32ce97ad76a81764a8
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Device Details

"Sterry" Manual Gastroenterology-Urology Surgical Instruments and Their Accessories (Sterilization)
TW: "ๅฒๆณฐ็‘ž" ๆ‰‹ๅ‹•ๅผ่ƒƒ่…ธ็ง‘-ๆณŒๅฐฟ็ง‘ๆ‰‹่ก“ๅ™จๆขฐๅŠๅ…ถ้™„ไปถ (ๆป…่Œ)
Risk Class 1

Registration Details

38ef89c2d9f28d32ce97ad76a81764a8

DHA09401885600

Company Information

Product Details

Limited to the first level identification scope of the classification and grading management method for medical equipment "Manual Gastroenterology-Urology Surgical Instruments and Their Accessories (H.4730)".

H Gastroenterology and urology

H.4730 H.4730 Hand Gastroentero-Urology Surgical Instruments and Accessories

import

Dates and Status

Mar 05, 2018

Mar 05, 2028