Japan PMDA registration 370077_219AKBZX00131000_A_01_08

Nightenor Wire

JP: ナイテノル　ワイヤー

Japan·MD·A5800·Updated August 01, 2024

Device classification / 分類

Device Type: MD
Device Class: A5800
Class Name (English): Orthodontic wire
Class Name (日本語): 歯列矯正用ワイヤ

Registration information / 登録情報

PMDA ID: 370077_219AKBZX00131000_A_01_08
Last Update Date: August 01, 2024
Official Documents: View PDF (PMDA)

Manufacturer / 製造販売業者

English: Manufacturing and sales: 3M Japan Innovation Co., Ltd.
日本語 (Japanese): 製造販売／スリーエムジャパンイノベーション株式会社

About this record

Access comprehensive regulatory information for Nightenor Wire (ナイテノル　ワイヤー) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 370077_219AKBZX00131000_A_01_08 and manufactured by Manufacturing and sales: 3M Japan Innovation Co., Ltd.. The device information was last updated on August 01, 2024.

This page provides complete registration details including device class (A5800), classification (Orthodontic wire / 歯列矯正用ワイヤ), manufacturer information (English and Japanese), and regulatory compliance data from the official Japan PMDA medical device database. Pure Global AI offers free bilingual access to Japan's complete medical device registry, helping global MedTech companies navigate PMDA regulations efficiently.

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