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“T&R” Nasal Mesh - Taiwan Registration b53efaa7f0c04560e41e6e86c6d5dad9

Access comprehensive regulatory information for “T&R” Nasal Mesh in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b53efaa7f0c04560e41e6e86c6d5dad9 and manufactured by T&R Biofab Co., Ltd.. The authorized representative in Taiwan is PRIMESTAR MEDICAL CO., 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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b53efaa7f0c04560e41e6e86c6d5dad9
Registration Details
Taiwan FDA Registration: b53efaa7f0c04560e41e6e86c6d5dad9
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Device Details

“T&R” Nasal Mesh
TW: “媞雅”鼻骨修補網片
Risk Class 2
MD

Registration Details

b53efaa7f0c04560e41e6e86c6d5dad9

Ministry of Health Medical Device Import No. 034261

DHA05603426106

Company Information

Korea, Republic of

Product Details

For details, it is Chinese approved copy of the imitation order

K Devices for neuroscience

K5300 Methyl methacrylate for craniomatomy

Imported from abroad

Dates and Status

Jan 14, 2021

Jan 14, 2026