Taiwan FDA registration 3764c073a626b7e5da0fd0a5be2d2b93
"Nara Seiko" Tendon sheath incision instrument (Non-Sterile)
TW: "奈良精工" 微創腱鞘切開器械組 (未滅菌)
Taiwan·Risk Class 1·MD·NARA SEIKO INC.·Registered Apr 05, 2017 – Apr 05, 2022ExpiredRegistration details
- Analysis ID
- 3764c073a626b7e5da0fd0a5be2d2b93
- License Form
- Ministry of Health Medical Device Import No. 017678
- Customs Code
- DHA09401767800
Company information
- Manufacturer
- NARA SEIKO INC.
- Manufacturer Country
- Japan
- Authorized Representative
- ORTHOLAND CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N4540 Manual osteologic surgery instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 05, 2017
- Expiry Date
- Apr 05, 2022
About this record
Access comprehensive regulatory information for "Nara Seiko" Tendon sheath incision 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 3764c073a626b7e5da0fd0a5be2d2b93 and manufactured by NARA SEIKO INC.. The authorized representative in Taiwan is ORTHOLAND CORPORATION.
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