Taiwan FDA registration adeb9d82cadbd3df4f429be2311e494d

"Hermon" manual instruments for general surgery (unsterilized)

TW: "赫蒙"一般手術用手動式器械(未滅菌)
Taiwan flagTaiwan·Risk Class 1·HANS HERMANN GMBH MEDIZINTEHNIK·Registered Apr 07, 2006 – Apr 07, 2011Cancelled
Registration details
Analysis ID
adeb9d82cadbd3df4f429be2311e494d
Customs Code
DHA04400348009
Company information
Manufacturer Country
Germany
Authorized Representative
BEAMED INSTRUMENTS CO., LTD.
Product details
Intended Use
Limited to the first level of the Measures for the Administration of Medical Devices (General Surgical Manual Instruments [I.4800])
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4800 Hand Instruments for General Surgery
Import Information
import
Dates and status
Registration Date
Apr 07, 2006
Expiry Date
Apr 07, 2011
Cancellation Date
Nov 27, 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 "Hermon" manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number adeb9d82cadbd3df4f429be2311e494d and manufactured by HANS HERMANN GMBH MEDIZINTEHNIK. The authorized representative in Taiwan is BEAMED INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HANS HERMANN GMBH MEDIZINTEHNIK, 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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