Taiwan FDA registration d350f45f253f0dd7c8f6d84b57ea8e93
"Schneihui" electric control system and its accessories
TW: “史耐輝”電動控制系統及其附件
Registration details
- Analysis ID
- d350f45f253f0dd7c8f6d84b57ea8e93
- Customs Code
- DHA00602105604
Company information
- Manufacturer
- SMITH & NEPHEW INC., ENDOSCOPY DIVISION
- Manufacturer Country
- United States
- Authorized Representative
- SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N 骨科學;; G 耳鼻喉科學
- Product Type (Level 2)
- G.4250 耳鼻喉電動式或氣動式外科鑽;; N.1100 關節鏡
- Import Information
- import
Dates and status
- Registration Date
- May 27, 2010
- Expiry Date
- May 27, 2025
About this record
Access comprehensive regulatory information for "Schneihui" electric control system and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d350f45f253f0dd7c8f6d84b57ea8e93 and manufactured by SMITH & NEPHEW INC., ENDOSCOPY DIVISION. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).
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.
Free DatabasePowered by Pure Global AI89,000+ Devices