Taiwan FDA registration 482218b9ad3975bc07d2e4abfb306d8b

HIRAM Abrasive device and accessories (Non-Sterile)

TW: 海勒 研磨裝置及其附件(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·HIRAM MEDICAL LIMITED·Registered Oct 01, 2021 – Oct 31, 2023Expired
Registration details
Analysis ID
482218b9ad3975bc07d2e4abfb306d8b
License Form
Ministry of Health Medical Device Import Registration No. 019525
Customs Code
DHA08401952502
Company information
Manufacturer Country
United Kingdom
Authorized Representative
Shili Biomedical Co., Ltd
Product details
Intended Use
Limited to the first level identification range of grinding devices and their accessories (F.6010) under the management measures for medical equipment.
Product Type (Level 1)
F Dental devices
Product Type (Level 2)
F6010 Grinding device and accessories
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2023
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About this record

Access comprehensive regulatory information for HIRAM Abrasive device and accessories (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 482218b9ad3975bc07d2e4abfb306d8b and manufactured by HIRAM MEDICAL LIMITED. The authorized representative in Taiwan is Shili Biomedical Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HIRAM MEDICAL LIMITED, 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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