Taiwan FDA registration 4aa201ac4233eb19f159d57ad155f3dc

"Ronamac" Olfactory Test Device (Non-Sterile)

TW: "朋笛" 嗅覺測試裝置 (未滅菌)

Taiwan·Risk Class 1·MD·GM INSTRUMENTS LTD.·Registered Nov 04, 2019 – Nov 04, 2024Expired

Registration details

Analysis ID: 4aa201ac4233eb19f159d57ad155f3dc
License Form: Ministry of Health Medical Device Import No. 021002
Customs Code: DHA09402100207

Company information

Manufacturer: GM INSTRUMENTS LTD.
Manufacturer Country: United Kingdom
Authorized Representative: RONAMAC INTERNATIONAL CORP.

Product details

Intended Use: Limited to the first level identification range of the "olfactory test device (G.1600)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1): G ENT device
Product Type (Level 2): G1600 olfactory test device
Import Information: Imported from abroad

Dates and status

Registration Date: Nov 04, 2019
Expiry Date: Nov 04, 2024

About this record

Access comprehensive regulatory information for "Ronamac" Olfactory Test Device (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 4aa201ac4233eb19f159d57ad155f3dc and manufactured by GM INSTRUMENTS LTD.. The authorized representative in Taiwan is RONAMAC INTERNATIONAL CORP..

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