Taiwan FDA registration e07b8bd4f6058b0db42dacf10fa6a109

"Schneefer" Walken electric knife probe

TW: “史耐輝”沃肯電刀用探頭
Taiwan flagTaiwan·Risk Class 2·ArthroCare Corporation;; SMITH & NEPHEW INC. ENDOSCOPY·Registered Jan 15, 2014 – Jan 15, 2029Active
Registration details
Analysis ID
e07b8bd4f6058b0db42dacf10fa6a109
Customs Code
DHA05602576000
Company information
Manufacturer Country
Costa Rica;;United States
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4400 Cutting and hemostasis electric knives and accessories thereof
Import Information
Contract manufacturing;; input
Dates and status
Registration Date
Jan 15, 2014
Expiry Date
Jan 15, 2029
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About this record

Access comprehensive regulatory information for "Schneefer" Walken electric knife probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e07b8bd4f6058b0db42dacf10fa6a109 and manufactured by ArthroCare Corporation;; SMITH & NEPHEW INC. ENDOSCOPY. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Venusa de Mexico S.A. de C.V;; SMITH & NEPHEW INC. ENDOSCOPY DIVISION, 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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