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“SRS Medical” The Spanner - Taiwan Registration 5b226ec4cdba18d44a6eb4a5c7ddc58f

Access comprehensive regulatory information for “SRS Medical” The Spanner in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 5b226ec4cdba18d44a6eb4a5c7ddc58f and manufactured by SRS MEDICAL. The authorized representative in Taiwan is REVO LASER CORPORATION.

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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5b226ec4cdba18d44a6eb4a5c7ddc58f
Registration Details
Taiwan FDA Registration: 5b226ec4cdba18d44a6eb4a5c7ddc58f
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Device Details

“SRS Medical” The Spanner
TW: “艾斯爾斯 麥迪克”史班那導尿支架組
Risk Class 3
MD

Registration Details

5b226ec4cdba18d44a6eb4a5c7ddc58f

Ministry of Health Medical Device Import No. 032717

DHA05603271700

Company Information

United States

Product Details

The Spammer is a temporary (up to 30 days) urine drainage device. To enable patients to urinate independently after minimally invasive treatment of benign prostatic hyperplasia (BPH) and urinary catheter insertion after surgery.

H Gastroenterology-urology devices

H9999 Other

Imported from abroad

Dates and Status

Aug 21, 2019

Aug 21, 2024