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"Guise" pulp power Diego power planer - Taiwan Registration 6e22a95bdf0c59f2674e2b85e1e8a50f

Access comprehensive regulatory information for "Guise" pulp power Diego power planer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6e22a95bdf0c59f2674e2b85e1e8a50f and manufactured by GYRUS ENT LLC. The authorized representative in Taiwan is MEDFRONT MEDICAL TECHNOLOGY CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GYRUS ENT LLC, A WHOLLY OWNED SUBSIDIARY OF GYRUS ACMI, INC., and 1 recent registrations in the same category. 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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6e22a95bdf0c59f2674e2b85e1e8a50f
Registration Details
Taiwan FDA Registration: 6e22a95bdf0c59f2674e2b85e1e8a50f
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Device Details

"Guise" pulp power Diego power planer
TW: "ๅ‰ๆ–ฏ"ๆผฟๅ‹•ๅŠ›่ฟชๅ“ฅๅ‹•ๅŠ›ๅˆจๅ‰ŠๆฉŸ
Risk Class 2
Cancelled

Registration Details

6e22a95bdf0c59f2674e2b85e1e8a50f

DHA00601695202

Company Information

United States

Product Details

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

G ENT Science

G.4250 ่€ณ้ผปๅ–‰้›ปๅ‹•ๅผๆˆ–ๆฐฃๅ‹•ๅผๅค–็ง‘้‘ฝ

import

Dates and Status

Aug 02, 2006

Aug 02, 2011

Oct 29, 2012

Cancellation Information

Logged out

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