Taiwan FDA registration c8306768e9c340da031e2cd4f80605cd

"Sterry" miniature biosensory forceps

TW: "史泰瑞" 微型生檢鉗
Taiwan flagTaiwan·Risk Class 2·STERIS CORPORATION;; UNITED STATES ENDOSCOPY GROUP, INC.·Registered Apr 16, 2021 – Apr 16, 2026Expired
Registration details
Analysis ID
c8306768e9c340da031e2cd4f80605cd
Customs Code
DHA05603443401
Company information
Manufacturer Country
United States
Authorized Representative
MEDTRUST INTERNATIONAL CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
H Gastroenterology and urology
Product Type (Level 2)
H.1075 腸胃科-泌尿科生檢器械
Import Information
import
Dates and status
Registration Date
Apr 16, 2021
Expiry Date
Apr 16, 2026
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About this record

Access comprehensive regulatory information for "Sterry" miniature biosensory forceps in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c8306768e9c340da031e2cd4f80605cd and manufactured by STERIS CORPORATION;; UNITED STATES ENDOSCOPY GROUP, INC.. The authorized representative in Taiwan is MEDTRUST INTERNATIONAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including STERIS CORPORATION;; UNITED STATES ENDOSCOPY GROUP, INC., and 1 recent registrations in the same category. 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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