Taiwan FDA registration 5b226ec4cdba18d44a6eb4a5c7ddc58f
“SRS Medical” The Spanner
TW: “艾斯爾斯 麥迪克”史班那導尿支架組
Registration details
- Analysis ID
- 5b226ec4cdba18d44a6eb4a5c7ddc58f
- License Form
- Ministry of Health Medical Device Import No. 032717
- Customs Code
- DHA05603271700
Company information
- Manufacturer
- SRS MEDICAL
- Manufacturer Country
- United States
- Authorized Representative
- REVO LASER CORPORATION
Product details
- Intended Use
- 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.
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H9999 Other
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 21, 2019
- Expiry Date
- Aug 21, 2024
About this record
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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