Taiwan FDA registration 53a417df20680f870d53fee08cd4de8a
“Zimmer” Allofit IT Alloclassic Acetabular Shell
TW: “捷邁”艾洛菲艾提人工髖臼杯
Taiwan·Risk Class 2·MD·ZIMMER GMBH·Registered Nov 10, 2014 – Nov 10, 2019CancelledRegistration details
- Analysis ID
- 53a417df20680f870d53fee08cd4de8a
- License Form
- Ministry of Health Medical Device Import No. 026778
- Customs Code
- DHA05602677808
Company information
- Manufacturer
- ZIMMER GMBH
- Manufacturer Country
- Switzerland
- Authorized Representative
- ZIMMER BIOMET TAIWAN CO., LTD.
Product details
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3350 Semi-restricted hip metal/polymer cement compound
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 10, 2014
- Expiry Date
- Nov 10, 2019
- 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 “Zimmer” Allofit IT Alloclassic Acetabular Shell in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 53a417df20680f870d53fee08cd4de8a and manufactured by ZIMMER GMBH. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..
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