Taiwan FDA registration 36f851b8dd73bfa6ec7657af5287eb64
"GACD" Ear, nose, and throat manual surgical instrument (Non-Sterile)
TW: "嘉克得" 耳鼻喉手動式外科器械 (未滅菌)
Taiwan·Risk Class 1·MD·GACD S.A.S.·Registered Aug 18, 2016 – Aug 18, 2021CancelledRegistration details
- Analysis ID
- 36f851b8dd73bfa6ec7657af5287eb64
- License Form
- Ministry of Health Medical Device Import No. 016906
- Customs Code
- DHA09401690605
Company information
- Manufacturer
- GACD S.A.S.
- Manufacturer Country
- France
- Authorized Representative
- RUI YAO DENTAL INTERNATIONAL TRADE 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
- Aug 18, 2016
- Expiry Date
- Aug 18, 2021
- 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 "GACD" 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 36f851b8dd73bfa6ec7657af5287eb64 and manufactured by GACD S.A.S.. The authorized representative in Taiwan is RUI YAO DENTAL INTERNATIONAL TRADE CO., LTD..
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices