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"ULTI MED" LH Ovulation Test (Non-Sterile) - Taiwan Registration c7485c2c579f071cf388b91d86aaed5e

Access comprehensive regulatory information for "ULTI MED" LH Ovulation Test (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 c7485c2c579f071cf388b91d86aaed5e and manufactured by ULTI MED PRODUCTS (DEUTSCHLAND) GMBH. The authorized representative in Taiwan is BioChain Co., Ltd..

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c7485c2c579f071cf388b91d86aaed5e
Registration Details
Taiwan FDA Registration: c7485c2c579f071cf388b91d86aaed5e
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Device Details

"ULTI MED" LH Ovulation Test (Non-Sterile)
TW: "็ˆพๅชž็พŽ"ๆŽ’ๅตๆชขๆธฌ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

c7485c2c579f071cf388b91d86aaed5e

Ministry of Health Medical Device Import No. 022302

DHA09402230201

Company Information

Product Details

Limited to the first level recognition range of the "Luteinizing hormone test system (A.1485)" of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A1485 Progesterone Test System

Imported from abroad

Dates and Status

Feb 05, 2021

Feb 05, 2026