Taiwan FDA registration 9fcda88e2b5272656498eb874ec3378b
“Skintact” Multifunction Defibrillation Electrode
TW: “施肯貼克”去顫器用電擊貼片
Taiwan·Risk Class 2·MD·LEONHARD LANG GMBH·Registered Aug 07, 2013 – Aug 07, 2018CancelledRegistration details
- Analysis ID
- 9fcda88e2b5272656498eb874ec3378b
- License Form
- Ministry of Health Medical Device Import No. 025222
- Customs Code
- DHA05602522208
Company information
- Manufacturer
- LEONHARD LANG GMBH
- Manufacturer Country
- Austria
- Authorized Representative
- SOPHYHZM MEDICAL INSTRUMENT CO., LTD.
Product details
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E5300 DC Defibrillator (with shock plate)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 07, 2013
- Expiry Date
- Aug 07, 2018
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “Skintact” Multifunction Defibrillation Electrode in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9fcda88e2b5272656498eb874ec3378b and manufactured by LEONHARD LANG GMBH. The authorized representative in Taiwan is SOPHYHZM MEDICAL INSTRUMENT CO., LTD..
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