Taiwan FDA registration 80f8d4c686e3f59e3211b98636eeed6e
"Pumei" hemorrhoid clamps
TW: "普美" 痔瘡夾鉗
Taiwan·Risk Class 1·PRO-MED INSTRUMENTE GMBH·Registered Nov 28, 2005 – Nov 28, 2010CancelledRegistration details
- Analysis ID
- 80f8d4c686e3f59e3211b98636eeed6e
- Customs Code
- DHA04400213704
Company information
- Manufacturer
- PRO-MED INSTRUMENTE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- WONDERFUL INSTRUMENTS COMPANY, LTD.
Product details
- Intended Use
- Surgical devices used in the gastroenterology department are non-electrical, hand-held or hand-operated.
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.4730 H.4730 Hand Gastroentero-Urology Surgical Instruments and Accessories
- Import Information
- import
Dates and status
- Registration Date
- Nov 28, 2005
- Expiry Date
- Nov 28, 2010
- Cancellation Date
- Jan 18, 2013
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Pumei" hemorrhoid clamps in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 80f8d4c686e3f59e3211b98636eeed6e and manufactured by PRO-MED INSTRUMENTE GMBH. The authorized representative in Taiwan is WONDERFUL INSTRUMENTS COMPANY, LTD..
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