Taiwan FDA registration 080dd36d37912ce25195a1841dc9926f
"Wallcenter" Manual surgical instrument for general use (Non-sterile)
TW: "沃生特"一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·MD·THE WALL CENTER·Registered Sep 15, 2015 – Sep 15, 2020CancelledRegistration details
- Analysis ID
- 080dd36d37912ce25195a1841dc9926f
- License Form
- Ministry of Health Medical Device Import No. 015676
- Customs Code
- DHA09401567609
Company information
- Manufacturer
- THE WALL CENTER
- Manufacturer Country
- United States
- Authorized Representative
- RUBY-JANE INTERNATIONAL CORPORATION
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 15, 2015
- Expiry Date
- Sep 15, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Wallcenter" Manual surgical instrument for general use (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 080dd36d37912ce25195a1841dc9926f and manufactured by THE WALL CENTER. The authorized representative in Taiwan is RUBY-JANE INTERNATIONAL CORPORATION.
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