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"THERAGUN" Manual cast application and removal instrument (non-sterile) - Taiwan Registration 4ba98d54ff67c6839764b0e0b3c57ad8

Access comprehensive regulatory information for "THERAGUN" Manual cast application and removal instrument (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 4ba98d54ff67c6839764b0e0b3c57ad8 and manufactured by THERAGUN LLC. The authorized representative in Taiwan is MEDEPOT 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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4ba98d54ff67c6839764b0e0b3c57ad8
Registration Details
Taiwan FDA Registration: 4ba98d54ff67c6839764b0e0b3c57ad8
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Device Details

"THERAGUN" Manual cast application and removal instrument (non-sterile)
TW: "็‰นๆ‹‰้‹ผ" ๆ‰‹ๅ‹•ๅผๆ‰“็Ÿณ่†ๅŠๆ‹†็Ÿณ่†ๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

4ba98d54ff67c6839764b0e0b3c57ad8

Ministry of Health Medical Device Import No. 018429

DHA09401842907

Company Information

United States

Product Details

Limited to the first level of identification scope of the Measures for the Administration of Medical Equipment "Manual Casting and Removal of Gypsum Removal Equipment (N.5980)".

N Orthopedic devices

N5980 Manual plaster casting and plaster removal equipment

Imported from abroad

Dates and Status

Oct 19, 2017

Oct 19, 2022