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NITTOBO r-GTP (Non-Sterile) - Taiwan Registration 25a0c8d318a7a58d3e2d365a3849508d

Access comprehensive regulatory information for NITTOBO r-GTP (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 25a0c8d318a7a58d3e2d365a3849508d and manufactured by NITTOBO MEDICAL CO., LTD. MEDICAL DEVELOPMENT CENTER. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.

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25a0c8d318a7a58d3e2d365a3849508d
Registration Details
Taiwan FDA Registration: 25a0c8d318a7a58d3e2d365a3849508d
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Device Details

NITTOBO r-GTP (Non-Sterile)
TW: ๆ—ฅๆฑ็ดก rโ€“้บฉ่ƒบ้†ฏ่ฝ‰็งป้…ถ่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

25a0c8d318a7a58d3e2d365a3849508d

Ministry of Health Medical Device Import No. 020846

DHA09402084602

Company Information

Product Details

Limited to the first level identification range of the measures for the administration of medical devices "r-glutamyl transferase (GGT) and isoenzyme test system (A.1360)".

A Clinical chemistry and clinical toxicology

A1360 r-glutamyl transferase (GGT) and isoenzyme test system

Imported from abroad

Dates and Status

Sep 10, 2019

Sep 10, 2024