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"STEMA" Non-Electric Biopsy Forceps (Non-Sterile) - Taiwan Registration 394e556f81422dbb59e9135235ede923

Access comprehensive regulatory information for "STEMA" Non-Electric Biopsy Forceps (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 394e556f81422dbb59e9135235ede923 and manufactured by STEMA MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is DERMACARE BIOMED INC..

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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394e556f81422dbb59e9135235ede923
Registration Details
Taiwan FDA Registration: 394e556f81422dbb59e9135235ede923
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Device Details

"STEMA" Non-Electric Biopsy Forceps (Non-Sterile)
TW: "ๆ€็‹„็‘ช"้ž้›ปๅ‹•ๆดป้ซ”็ต„็น”ๅคพ(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

394e556f81422dbb59e9135235ede923

Ministry of Health Medical Device Import No. 019178

DHA09401917800

Company Information

Germany

Product Details

H Gastroenterology-urology devices

H1075 Gastroenterology - Urology biopsy instruments

Imported from abroad

Dates and Status

Jun 13, 2018

Jun 13, 2023

Jan 18, 2023

Cancellation Information

Logged out

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