Taiwan FDA registration a0d77339cd9903ec7993c4eb46524983
"Interwa" Jerry ENT Manual Surgical Instruments (Unsterilized)
TW: "英特華" 傑瑞耳鼻喉手動式外科器械 (未滅菌)
Registration details
- Analysis ID
- a0d77339cd9903ec7993c4eb46524983
- Customs Code
- DHA04401065904
Company information
- Manufacturer
- INTEGRA YORK PA, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Huizhong Co., Ltd
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Manual Surgical Instruments (G.4420)".
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4420 Otolaryngology manual surgical instruments
- Import Information
- import
Dates and status
- Registration Date
- Aug 01, 2011
- Expiry Date
- Aug 01, 2021
- Cancellation Date
- Oct 06, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Interwa" Jerry ENT Manual Surgical Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a0d77339cd9903ec7993c4eb46524983 and manufactured by INTEGRA YORK PA, INC.. The authorized representative in Taiwan is Huizhong 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