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"Luther" orthopedic manual arthroscopic equipment (unsterilized) - Taiwan Registration dd0871f642f0013e3216ffe0da6dc8ad

Access comprehensive regulatory information for "Luther" orthopedic manual arthroscopic equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dd0871f642f0013e3216ffe0da6dc8ad and manufactured by LUT GMBH. The authorized representative in Taiwan is REVO LASER CORPORATION.

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dd0871f642f0013e3216ffe0da6dc8ad
Registration Details
Taiwan FDA Registration: dd0871f642f0013e3216ffe0da6dc8ad
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Device Details

"Luther" orthopedic manual arthroscopic equipment (unsterilized)
TW: โ€œ่ทฏๅพทโ€้ชจ็ง‘ๆ‰‹ๅ‹•ๅผ้—œ็ฏ€้กๅ™จๆ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

dd0871f642f0013e3216ffe0da6dc8ad

DHA04400788401

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 Orthopedics

N.1100 Closing Lenses

import

Dates and Status

Jul 03, 2009

Jul 03, 2014

Jun 25, 2018

Cancellation Information

Logged out

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