Manual instrument for general surgery (unsterilized)
Taiwan·Risk Class 1·DI CHENG RUBBER INDUSTRIES INC.·Registered Mar 18, 2011 – Mar 18, 2016Cancelled- Analysis ID
- 76d02a87d089e9330da6e4d24e2b356e
- Manufacturer
- DI CHENG RUBBER INDUSTRIES INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- DI CHENG RUBBER INDUSTRIES INC.
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- Domestic
- Registration Date
- Mar 18, 2011
- Expiry Date
- Mar 18, 2016
- Cancellation Date
- Jul 31, 2018
- Status
- Logged out
- Reason
- 未展延而逾期者
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Access comprehensive regulatory information for Manual instrument for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 76d02a87d089e9330da6e4d24e2b356e and manufactured by DI CHENG RUBBER INDUSTRIES INC.. The authorized representative in Taiwan is DI CHENG RUBBER INDUSTRIES INC..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including EUROMI S.A., Gray Surgical, and 2 recent registrations in the same category. 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.