Taiwan FDA registration ee6cf33071b91cc7c2a4d6a4f1c9f574

BIOMOLD Synthetic Bone Graft

TW: 拜莫特生物可吸收補骨物

Taiwan·Risk Class 2·MD·İDEA İLAÇ ÜRETİM SANAYİ LTD. ŞTİ·Registered Jun 10, 2022 – Jun 10, 2027Active

Registration details

Analysis ID: ee6cf33071b91cc7c2a4d6a4f1c9f574
License Form: Ministry of Health Medical Device Import No. 035576
Customs Code: DHA05603557600

Company information

Manufacturer: İDEA İLAÇ ÜRETİM SANAYİ LTD. ŞTİ
Manufacturer Country: Turkey
Authorized Representative: XELITE BIOMED LTD.

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N3045 Absorbable calcium salt bone cavity filling device
Import Information: Imported from abroad

Dates and status

Registration Date: Jun 10, 2022
Expiry Date: Jun 10, 2027

About this record

Access comprehensive regulatory information for BIOMOLD Synthetic Bone Graft in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ee6cf33071b91cc7c2a4d6a4f1c9f574 and manufactured by İDEA İLAÇ ÜRETİM SANAYİ LTD. ŞTİ. The authorized representative in Taiwan is XELITE BIOMED LTD..

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