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"Bolma" Imo segmented laser - Taiwan Registration 72ba29fb6cc5245e1ec6bae14afcd532

Access comprehensive regulatory information for "Bolma" Imo segmented laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 72ba29fb6cc5245e1ec6bae14afcd532 and manufactured by PALOMAR MEDICAL PRODUCTS INC.. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..

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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72ba29fb6cc5245e1ec6bae14afcd532
Registration Details
Taiwan FDA Registration: 72ba29fb6cc5245e1ec6bae14afcd532
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Device Details

"Bolma" Imo segmented laser
TW: โ€œๅฏถๆจ‚็‘ชโ€ไผŠ่Žซๅˆ†ๆฎตๅผ้›ทๅฐ„ๅ„€
Risk Class 2
Cancelled

Registration Details

72ba29fb6cc5245e1ec6bae14afcd532

DHA00602500303

Company Information

United States

Product Details

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

I General, Plastic Surgery and Dermatology

I.4810 Lasers for general surgical, orthopaedic and dermatological use

import

Dates and Status

May 08, 2013

May 08, 2018

Dec 09, 2019

Cancellation Information

Logged out

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