Taiwan FDA registration 2e8a0e8750cbae01c945f70f59573b92

"Wardman" light healer

TW: “沃德曼”光線治療器
Taiwan flagTaiwan·Risk Class 2·HERBERT WALDMANN GMBH& CO. KG·Registered Dec 28, 2012 – Dec 28, 2017Cancelled
Registration details
Analysis ID
2e8a0e8750cbae01c945f70f59573b92
Customs Code
DHA00602437101
Company information
Manufacturer Country
Germany
Authorized Representative
TRUSHINE MEDICAL INSTRUMENT CO., LTD.
Product details
Intended Use
Restricted to the treatment of acne (acne) (ACNE).
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4630 皮膚病用紫外線燈
Import Information
import
Dates and status
Registration Date
Dec 28, 2012
Expiry Date
Dec 28, 2017
Cancellation Date
Dec 19, 2017
Cancellation information
Status
Logged out
Reason
自請註銷
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About this record

Access comprehensive regulatory information for "Wardman" light healer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2e8a0e8750cbae01c945f70f59573b92 and manufactured by HERBERT WALDMANN GMBH& CO. KG. The authorized representative in Taiwan is TRUSHINE MEDICAL INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HERBERT WALDMANN GMBH& CO. KG, 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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