"Integra" Manual surgical instrument for general use (Non-Sterile)
Taiwan·Risk Class 1·MD·INTEGRA YORK PA, INC.·Registered Dec 31, 2015 – Dec 31, 2020Cancelled- Analysis ID
- 86b85b677bdb36c4f2b7b42acc8b3618
- License Form
- Ministry of Health Medical Device Import No. 016041
- Customs Code
- DHA09401604100
- Manufacturer
- INTEGRA YORK PA, INC.
- Manufacturer Country
- United States
- Authorized Representative
- KINDMED CORPORATION
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
- Registration Date
- Dec 31, 2015
- Expiry Date
- Dec 31, 2020
- Cancellation Date
- Aug 05, 2022
- Status
- Logged out
- Reason
- 未展延而逾期者
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Access comprehensive regulatory information for "Integra" Manual surgical instrument for general use (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 86b85b677bdb36c4f2b7b42acc8b3618 and manufactured by INTEGRA YORK PA, INC.. The authorized representative in Taiwan is KINDMED CORPORATION.
This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including Integra LifeSciences Production Corporation, INTEGRA YORK PA, INC., and 5 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.