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"Difu Spine" Fronti Scoliosis Correction System - Taiwan Registration 1812f0b0d732d718da003254de7d6cfa

Access comprehensive regulatory information for "Difu Spine" Fronti Scoliosis Correction System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1812f0b0d732d718da003254de7d6cfa and manufactured by DEPUY SPINE, INC.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details. 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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1812f0b0d732d718da003254de7d6cfa
Registration Details
Taiwan FDA Registration: 1812f0b0d732d718da003254de7d6cfa
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Device Details

"Difu Spine" Fronti Scoliosis Correction System
TW: "ๅธๅฏŒ่„ŠๆคŽ" ไฝ›ๆœ—ๅธ่„ŠๆŸฑๅดๅฝŽๅ‰ๆ–น็Ÿฏๆฒป็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

1812f0b0d732d718da003254de7d6cfa

DHA00601022707

Company Information

United States

Product Details

Vacuum.

N Orthopedics

import

Dates and Status

Feb 25, 2003

Feb 25, 2018

Nov 04, 2019

Cancellation Information

Logged out

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