Pure Global

"Sunover" waste collection bag (unsterilized) - Taiwan Registration 0449aab91e1956167d3526c5e9d699ab

Access comprehensive regulatory information for "Sunover" waste collection bag (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0449aab91e1956167d3526c5e9d699ab and manufactured by HISPA MEDICAL & EQUIPMENT(GZ) CO., LTD. The authorized representative in Taiwan is Sunray Health 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
0449aab91e1956167d3526c5e9d699ab
Registration Details
Taiwan FDA Registration: 0449aab91e1956167d3526c5e9d699ab
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Sunover" waste collection bag (unsterilized)
TW: "ๆ—ฅๆบข" ๅปขๆถฒๆ”ถ้›†่ข‹ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

0449aab91e1956167d3526c5e9d699ab

DHA09600204406

Company Information

Product Details

Limited to the first level of identification scope of "non-powered, single-patient, portable suction device (I.4680)" under the Measures for the Administration of Medical Devices.

I General, Plastic Surgery and Dermatology

I.4680 Non-motive, single patient-use, carry-on suctioning device

Chinese goods;; input

Dates and Status

Dec 25, 2013

Dec 25, 2018

Jul 15, 2022

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€