Taiwan FDA registration 72043d9fe104f10d9267122841c1004c
Inami manual ophthalmic surgical instrument (unsterile)
TW: 井浪手動式眼科手術器械 (未滅菌)
Registration details
- Analysis ID
- 72043d9fe104f10d9267122841c1004c
- Customs Code
- DHA04400251905
Company information
- Manufacturer
- INAMI & CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- TAI SHING INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Manual eye surgery instruments are non-electric, hand-held devices designed to assist or perform eye surgery.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4350 手動式眼科手術器械
- Import Information
- import
Dates and status
- Registration Date
- Jan 13, 2006
- Expiry Date
- Jan 13, 2026
About this record
Access comprehensive regulatory information for Inami manual ophthalmic surgical instrument (unsterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 72043d9fe104f10d9267122841c1004c and manufactured by INAMI & CO., LTD.. The authorized representative in Taiwan is TAI SHING INSTRUMENTS 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.
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