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"Shirley" manual arthroscopic equipment (unsterilized) - Taiwan Registration ccad5d5ea995b29b3d0b558576f24ef7

Access comprehensive regulatory information for "Shirley" 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 ccad5d5ea995b29b3d0b558576f24ef7 and manufactured by SCHOLLY FIBEROPTIC GMBH. The authorized representative in Taiwan is REVO LASER 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.

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ccad5d5ea995b29b3d0b558576f24ef7
Registration Details
Taiwan FDA Registration: ccad5d5ea995b29b3d0b558576f24ef7
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Device Details

"Shirley" manual arthroscopic equipment (unsterilized)
TW: โ€œ้›ช่މโ€ๆ‰‹ๅ‹•ๅผ้—œ็ฏ€้กๅ™จๆ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

ccad5d5ea995b29b3d0b558576f24ef7

DHA04400536608

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

Nov 22, 2006

Nov 22, 2011

Nov 19, 2012

Cancellation Information

Logged out

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