Taiwan FDA registration 9b3f5ecc6b3ebb06ed0781dee58b20b7

Ammora Warm Patch (Unsterilized)

TW: 安摩樂 溫熱敷貼片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·HEFEI KOBAYASHI DAILY PRODUCTS CO., LTD.·Registered Sep 11, 2014 – Sep 11, 2029Active
Registration details
Analysis ID
9b3f5ecc6b3ebb06ed0781dee58b20b7
Customs Code
DHA09600221609
Company information
Manufacturer Country
China
Product details
Intended Use
Limited to the classification and grading management of medical equipment, the first level identification range of "Discardable Hot and Cold Compress Packs for Medical Use (O.5710)".
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.5710 醫療用可丟棄式的冷熱敷包
Import Information
Chinese goods;; input
Dates and status
Registration Date
Sep 11, 2014
Expiry Date
Sep 11, 2029
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About this record

Access comprehensive regulatory information for Ammora Warm Patch (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9b3f5ecc6b3ebb06ed0781dee58b20b7 and manufactured by HEFEI KOBAYASHI DAILY PRODUCTS CO., LTD.. The authorized representative in Taiwan is KOBAYASHI PHARMACEUTICAL (TAIWAN) CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SHANGHAI KOBAYASHI DAILY CHEMICALS CO., LTD., and 1 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.

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