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"Aloft" is a pneumatic multi-haired suture clamp with titanium pneumatics - Taiwan Registration 9c78673a0e139524431df4db2af35989

Access comprehensive regulatory information for "Aloft" is a pneumatic multi-haired suture clamp with titanium pneumatics in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9c78673a0e139524431df4db2af35989 and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..

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9c78673a0e139524431df4db2af35989
Registration Details
Taiwan FDA Registration: 9c78673a0e139524431df4db2af35989
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Device Details

"Aloft" is a pneumatic multi-haired suture clamp with titanium pneumatics
TW: โ€œ้›…ๆฐโ€ๅทงๆŽ„้ˆฆ้‡‘ๅฑฌๆฐฃๅ‹•ๅฏ้‡่ค‡ไฝฟ็”จๅคš็™ผๅผ็ธซๅˆๅคพ
Risk Class 2

Registration Details

9c78673a0e139524431df4db2af35989

DHA05603235801

Company Information

Germany

Product Details

For details, it is Chinese approved copy of the imitation order

I General, Plastic Surgery and Dermatology

I.4300 Implantable Clips

import

Dates and Status

Mar 28, 2019

Mar 28, 2029