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"Maxer" Spinal Endoscopic Instruments (Non-Sterile) - Taiwan Registration c4605fc73d670dfc5a94e4d67f991297

Access comprehensive regulatory information for "Maxer" Spinal Endoscopic Instruments (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c4605fc73d670dfc5a94e4d67f991297 and manufactured by MAXER MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is Ramo International Limited.

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c4605fc73d670dfc5a94e4d67f991297
Registration Details
Taiwan FDA Registration: c4605fc73d670dfc5a94e4d67f991297
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Device Details

"Maxer" Spinal Endoscopic Instruments (Non-Sterile)
TW: "้บฅๅ…‹ๆ–ฏ" ่„ŠๆคŽๅ…ง่ฆ–้กๅทฅๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

c4605fc73d670dfc5a94e4d67f991297

Ministry of Health Medical Device Import No. 017291

DHA09401729102

Company Information

Germany

Product Details

Limited to the first level identification range of "Arthroscopy (N.1100)" of the Measures for the Administration of Medical Equipment.

N Orthopedic devices

N1100 Arthroscopy

Imported from abroad

Dates and Status

Dec 16, 2016

Dec 16, 2021