Taiwan FDA registration e703bcde8960dd4c889877745611ddd2

"Yongchang" plaster removal equipment (unsterilized)

TW: “永昌”石膏拆除器械 (未滅菌)

Taiwan·Risk Class 1·SHANGHAI MEDICAL INSTRAMENTS (GROUP) CO., LTD.·Registered Oct 29, 2008 – Oct 29, 2023Expired

Registration details

Analysis ID: e703bcde8960dd4c889877745611ddd2
Customs Code: DHA04600058906

Company information

Manufacturer: SHANGHAI MEDICAL INSTRAMENTS (GROUP) CO., LTD.
Manufacturer Country: China
Authorized Representative: SUNMED INSTRUMENTS CO.

Product details

Intended Use: Limited to the classification and grading management measures for medical equipment, gypsum removal equipment (N.5960) first grade identification range.
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N.5960 石膏拆除器械
Import Information: Chinese goods;; input

Dates and status

Registration Date: Oct 29, 2008
Expiry Date: Oct 29, 2023

About this record

Access comprehensive regulatory information for "Yongchang" plaster removal equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e703bcde8960dd4c889877745611ddd2 and manufactured by SHANGHAI MEDICAL INSTRAMENTS (GROUP) CO., LTD.. The authorized representative in Taiwan is SUNMED INSTRUMENTS CO..

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