Taiwan FDA registration 1deee5cdcf59b4e4353fc8a3ddb72379
“BMA” Disposable Polypectomy Snare
TW: “必恩”拋棄式息肉切除器
Registration details
- Analysis ID
- 1deee5cdcf59b4e4353fc8a3ddb72379
- License Form
- Ministry of Health Medical Device Import No. 035815
- Customs Code
- DHA05603581502
Company information
- Manufacturer
- BMA Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- WELMORE CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H4300 Electrosurgical device for endoscopes and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 22, 2022
- Expiry Date
- Aug 22, 2027
About this record
Access comprehensive regulatory information for “BMA” Disposable Polypectomy Snare in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1deee5cdcf59b4e4353fc8a3ddb72379 and manufactured by BMA Co., Ltd.. The authorized representative in Taiwan is WELMORE CO., LTD..
This page provides complete technical specifications, regulatory compliance details. 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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