“Stryker” CrossFlow Integrated Arthroscopy Pump - Taiwan Registration d06d98e9e361bbcd21a4f18a8182a922
Access comprehensive regulatory information for “Stryker” CrossFlow Integrated Arthroscopy Pump in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d06d98e9e361bbcd21a4f18a8182a922 and manufactured by STRYKER ENDOSCOPY. The authorized representative in Taiwan is Stryker (Far East) Co., Ltd. Taiwan Branch.
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.
Device Details
Registration Details
d06d98e9e361bbcd21a4f18a8182a922
Ministry of Health Medical Device Import No. 036016
DHA05603601603
Product Details
Details are as detailed as approved Chinese instructions
N Orthopedics
N1100 Arthroscopy
Imported from abroad
Dates and Status
Oct 31, 2022
Oct 31, 2027

