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Taiwan FDA registration f3cbcf026e2ec370cbfea46251067609

Universal hydroxide apatite bone graft cement

TW: 合普適氫氧磷灰石骨移植膠泥
Taiwan flagTaiwan·LIFECORE BIOMEDUCAL, INC. ORAL RESTORATIVE DIVISION·Registered Sep 11, 1993 – Sep 11, 1998Cancelled
Registration details
Analysis ID
f3cbcf026e2ec370cbfea46251067609
Customs Code
DHA00600699804
Company information
Manufacturer
LIFECORE BIOMEDUCAL, INC. ORAL RESTORATIVE DIVISION
Manufacturer Country
United States
Authorized Representative
Bowling Drug Instruments Co., Ltd
Product details
Intended Use
The details are as detailed as the approved copy of the imitation label
Product Type (Level 1)
0399 Other artificial function substitutes
Import Information
import
Dates and status
Registration Date
Sep 11, 1993
Expiry Date
Sep 11, 1998
Cancellation Date
Aug 24, 2000
Cancellation information
Status
Logged out
Reason
未展延而逾期者
About this record

Access comprehensive regulatory information for Universal hydroxide apatite bone graft cement in Taiwan's medical device market through Pure Global AI's free database. is registered under number f3cbcf026e2ec370cbfea46251067609 and manufactured by LIFECORE BIOMEDUCAL, INC. ORAL RESTORATIVE DIVISION. The authorized representative in Taiwan is Bowling Drug Instruments Co., Ltd.

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