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"Nara Seiko" Tendon sheath incision instrument (Non-Sterile) - Taiwan Registration 3764c073a626b7e5da0fd0a5be2d2b93

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.

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3764c073a626b7e5da0fd0a5be2d2b93
Registration Details
Taiwan FDA Registration: 3764c073a626b7e5da0fd0a5be2d2b93
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Device Details

"Nara Seiko" Tendon sheath incision instrument (Non-Sterile)
TW: "ๅฅˆ่‰ฏ็ฒพๅทฅ" ๅพฎๅ‰ต่…ฑ้ž˜ๅˆ‡้–‹ๅ™จๆขฐ็ต„ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

3764c073a626b7e5da0fd0a5be2d2b93

Ministry of Health Medical Device Import No. 017678

DHA09401767800

Company Information

Japan

Product Details

Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.

N Orthopedic devices

N4540 Manual osteologic surgery instrument

Imported from abroad

Dates and Status

Apr 05, 2017

Apr 05, 2022