Taiwan FDA registration 890e4f154117e125e96e0bd3ee1e6aa4

"Stoddard" Abrasive Device and Accessories (Non-Sterile)

TW: "斯托達德" 研磨裝置及其附件(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·STODDARD MANUFACTURING COMPANY LIMITED·Registered Oct 01, 2021 – Oct 31, 2026Active
Registration details
Analysis ID
890e4f154117e125e96e0bd3ee1e6aa4
License Form
Ministry of Health Medical Device Import Registration No. 016163
Customs Code
DHA08401616302
Company information
Manufacturer Country
United Kingdom
Authorized Representative
CHIH SHIH TRADING CO., LTD.
Product details
Intended Use
Limited to the first level identification range of grinding devices and their accessories (F.6010) under the management measures for medical equipment.
Product Type (Level 1)
F Dental devices
Product Type (Level 2)
F6010 Grinding device and accessories
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2026
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About this record

Access comprehensive regulatory information for "Stoddard" Abrasive Device and Accessories (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 890e4f154117e125e96e0bd3ee1e6aa4 and manufactured by STODDARD MANUFACTURING COMPANY LIMITED. The authorized representative in Taiwan is CHIH SHIH TRADING CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including STODDARD MANUFACTURING COMPANY LIMITED, and 2 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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