Taiwan FDA registration 0cb9a16a2e458e7a2a859ecd52389c05
"Squip" Ear, nose, and throat manual surgical instrument (Non-sterile)
TW: "適瑰寶"耳鼻喉手動式外科器械 (未滅菌)
Taiwan·Risk Class 1·MD·SQUIP, INC.·Registered Jan 09, 2015 – Jan 09, 2020CancelledRegistration details
- Analysis ID
- 0cb9a16a2e458e7a2a859ecd52389c05
- License Form
- Ministry of Health Medical Device Import No. 014832
- Customs Code
- DHA09401483205
Company information
- Manufacturer
- SQUIP, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ANGEL MEDICAL INSTRUMENT CO., LTD.
Product details
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4420 OTOLARYNGARY Manual Surgical Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 09, 2015
- Expiry Date
- Jan 09, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
About this record
Access comprehensive regulatory information for "Squip" Ear, nose, and throat manual surgical instrument (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0cb9a16a2e458e7a2a859ecd52389c05 and manufactured by SQUIP, INC.. The authorized representative in Taiwan is ANGEL MEDICAL INSTRUMENT CO., LTD..
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