Taiwan FDA registration 504a5890eafa967b4cbca04e1b34fa2a
“BIOPLATE” Preformed Fixation System
TW: “拜普雷”預成形固定系統
Taiwan·Risk Class 2·MD·BIOPLATE, INC.·Registered Oct 17, 2016 – Oct 17, 2026ActiveRegistration details
- Analysis ID
- 504a5890eafa967b4cbca04e1b34fa2a
- License Form
- Ministry of Health Medical Device Import No. 028985
- Customs Code
- DHA05602898500
Company information
- Manufacturer
- BIOPLATE, INC.
- Manufacturer Country
- United States
- Authorized Representative
- MATECH HEALTHCARE CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K5330 Preformed Immutable Head Moulding Plate
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 17, 2016
- Expiry Date
- Oct 17, 2026
About this record
Access comprehensive regulatory information for “BIOPLATE” Preformed Fixation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 504a5890eafa967b4cbca04e1b34fa2a and manufactured by BIOPLATE, INC.. The authorized representative in Taiwan is MATECH HEALTHCARE CORPORATION.
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