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"Maxell" Abdominal Inflator Accessory (Unsterilized) - Taiwan Registration 5ab3c1909dd85863aa529eb749c7879b

Access comprehensive regulatory information for "Maxell" Abdominal Inflator Accessory (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5ab3c1909dd85863aa529eb749c7879b and manufactured by MAXER MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is HIGH TOP MEDICAL 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.

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5ab3c1909dd85863aa529eb749c7879b
Registration Details
Taiwan FDA Registration: 5ab3c1909dd85863aa529eb749c7879b
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Device Details

"Maxell" Abdominal Inflator Accessory (Unsterilized)
TW: "้บฅๅ…‹ๆ–ฏ็ˆพ" ่…น่…”ๅ……ๆฐฃๆฉŸ้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

5ab3c1909dd85863aa529eb749c7879b

DHA04401219600

Company Information

Germany

Product Details

Limited to the first level recognition range of laparoscopic perfusion device (L.1730) for the management of medical devices.

l Obstetrics and Gynecology

L.1730 ่…น่…”้ก็Œๅ…ฅๅ™จ

import

Dates and Status

Sep 21, 2012

Sep 21, 2022

Apr 12, 2024

Cancellation Information

Logged out

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