Pure Global

Tripping film type liquid tripping paste (unsterilized) - Taiwan Registration bd5eeed632ad55a4c4a7f4c298bbd7f8

Access comprehensive regulatory information for Tripping film type liquid tripping paste (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bd5eeed632ad55a4c4a7f4c298bbd7f8 and manufactured by OHKI PHARMACEUTICAL CO., LTD.. The authorized representative in Taiwan is TEN SUN PHARMA COMPANY LIMITED.

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
bd5eeed632ad55a4c4a7f4c298bbd7f8
Registration Details
Taiwan FDA Registration: bd5eeed632ad55a4c4a7f4c298bbd7f8
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Tripping film type liquid tripping paste (unsterilized)
TW: ๆต็ต†่–„่†œๅž‹ๆถฒ้ซ”็ต†ๅ‰ต่†(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

bd5eeed632ad55a4c4a7f4c298bbd7f8

DHA04401028900

Company Information

Product Details

Limit the first level identification range of liquid bandages (J.5090) of the Measures for the Administration of Medical Devices.

J General hospital and personal use equipment

J.5090 Liquid bandages

import

Dates and Status

Apr 29, 2011

Apr 29, 2016

Jul 31, 2018

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€