Taiwan FDA registration 3e3f5e871e4ead2dfb1c1a0a58f0169b
"Cottmann Schuttloff" in vitro drainage system
TW: "柯特曼舒特樂夫" 體外引流系統
Taiwan·Risk Class 2·MEDOS SARL;; CODMAN & SHURTLEFF,INC.·Registered Jun 24, 2005 – Jun 24, 2020CancelledRegistration details
- Analysis ID
- 3e3f5e871e4ead2dfb1c1a0a58f0169b
- Customs Code
- DHA00601152201
Company information
- Manufacturer
- MEDOS SARL;; CODMAN & SHURTLEFF,INC.
- Manufacturer Country
- United States;;Switzerland
- Authorized Representative
- K&C MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Neuroscience
- Import Information
- import
Dates and status
- Registration Date
- Jun 24, 2005
- Expiry Date
- Jun 24, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Cottmann Schuttloff" in vitro drainage system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3e3f5e871e4ead2dfb1c1a0a58f0169b and manufactured by MEDOS SARL;; CODMAN & SHURTLEFF,INC.. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
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