Taiwan FDA registration 41fea96dcd3afd8031b1cf04a60467f7

"Meril" Mesire Sinus Balloon Catheter & Sinus Guide Catheter(Sterile)

TW: "美瑞爾" 鼻竇氣球導管及鼻竇導引導管 (滅菌)

Taiwan·Risk Class 1·MD·Meril Life Sciences Pvt. Ltd.·Registered Dec 01, 2016 – Dec 01, 2026Active

Registration details

Analysis ID: 41fea96dcd3afd8031b1cf04a60467f7
License Form: Ministry of Health Medical Device Import No. 017240
Customs Code: DHA09401724008

Company information

Manufacturer: Meril Life Sciences Pvt. Ltd.
Manufacturer Country: India
Authorized Representative: MIRACOLO BIOTECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Manual Surgical Instruments (G.4420)".
Product Type (Level 1): G ENT device
Product Type (Level 2): G4420 OTOLARYNGARY Manual Surgical Instrument
Import Information: Imported from abroad; GMP

Dates and status

Registration Date: Dec 01, 2016
Expiry Date: Dec 01, 2026

About this record

Access comprehensive regulatory information for "Meril" Mesire Sinus Balloon Catheter & Sinus Guide Catheter(Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 41fea96dcd3afd8031b1cf04a60467f7 and manufactured by Meril Life Sciences Pvt. Ltd.. The authorized representative in Taiwan is MIRACOLO BIOTECHNOLOGY CO., LTD..

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