Pure Global

"Kemel" syringe rack (unsterilized) - Taiwan Registration 21278ede74a1157f402440bf07623263

Access comprehensive regulatory information for "Kemel" syringe rack (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 21278ede74a1157f402440bf07623263 and manufactured by CARMEL PHARMA AB. The authorized representative in Taiwan is MEDFRONT MEDICAL TECHNOLOGY 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
21278ede74a1157f402440bf07623263
Registration Details
Taiwan FDA Registration: 21278ede74a1157f402440bf07623263
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Kemel" syringe rack (unsterilized)
TW: โ€œๅฏ็พŽ็ˆพโ€ ๆณจๅฐ„ๆžถ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

21278ede74a1157f402440bf07623263

DHA04400889001

Company Information

Sweden

Product Details

Limited to the first level identification range of the "Injection Rack (J.6990)" of the Measures for the Administration of Medical Equipment.

J General hospital and personal use equipment

J.6990 Injection holder

import

Dates and Status

Jun 09, 2010

Jun 09, 2015

Jul 02, 2018

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ