Pure Global

"Snowden Pencer/ V. Mueller" Manual surgical instrument for general use (Non-Sterile) - Taiwan Registration 4ee252e017641d957b7d156b21e360bb

Access comprehensive regulatory information for "Snowden Pencer/ V. Mueller" Manual surgical instrument for general use (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 4ee252e017641d957b7d156b21e360bb and manufactured by CAREFUSION GERMANY 318 GMBH. The authorized representative in Taiwan is DOUBLE-SUCCESS 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
4ee252e017641d957b7d156b21e360bb
Registration Details
Taiwan FDA Registration: 4ee252e017641d957b7d156b21e360bb
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Snowden Pencer/ V. Mueller" Manual surgical instrument for general use (Non-Sterile)
TW: "ๅฒ่ซพ้ “่ณ“ๅฃซ/็ฑณ็ฉ†ๅ‹’" ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

4ee252e017641d957b7d156b21e360bb

Ministry of Health Medical Device Import No. 019200

DHA09401920006

Company Information

Germany

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad

Dates and Status

Jun 20, 2018

Jun 20, 2023