Taiwan FDA registration ba58112ada0c6aaba320d3ded1c1c4e4

Hydroxide apatite

TW: 氫氧磷灰石
Taiwan flagTaiwan·LIFECORE BIOMEDUCAL, INC. ORAL RESTORATIVE DIVISION·Registered Dec 29, 1992 – Dec 29, 1997Cancelled
Registration details
Analysis ID
ba58112ada0c6aaba320d3ded1c1c4e4
Customs Code
DHA00600682703
Company information
Manufacturer Country
United States
Authorized Representative
Bowling Drug Instruments Co., Ltd
Product details
Product Type (Level 1)
0399 Other artificial function substitutes
Import Information
import
Dates and status
Registration Date
Dec 29, 1992
Expiry Date
Dec 29, 1997
Cancellation Date
Aug 24, 2000
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for Hydroxide apatite in Taiwan's medical device market through Pure Global AI's free database. is registered under number ba58112ada0c6aaba320d3ded1c1c4e4 and manufactured by LIFECORE BIOMEDUCAL, INC. ORAL RESTORATIVE DIVISION. The authorized representative in Taiwan is Bowling Drug Instruments Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including LIFECORE BIOMEDUCAL, INC. ORAL RESTORATIVE DIVISION, NOBEL BIOCARE USA, INC, and 3 recent registrations in the same category. 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.

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