Taiwan FDA registration 6e22a95bdf0c59f2674e2b85e1e8a50f

"Guise" pulp power Diego power planer

TW: "吉斯"漿動力迪哥動力刨削機
Taiwan flagTaiwan·Risk Class 2·GYRUS ENT LLC·Registered Aug 02, 2006 – Aug 02, 2011Cancelled
Registration details
Analysis ID
6e22a95bdf0c59f2674e2b85e1e8a50f
Customs Code
DHA00601695202
Company information
Manufacturer
GYRUS ENT LLC
Manufacturer Country
United States
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
G ENT Science
Product Type (Level 2)
G.4250 耳鼻喉電動式或氣動式外科鑽
Import Information
import
Dates and status
Registration Date
Aug 02, 2006
Expiry Date
Aug 02, 2011
Cancellation Date
Oct 29, 2012
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

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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