Taiwan FDA registration e28411eb149de981013703a9eecc5202

Nitto spinning ammonia reagent-correction solution

TW: 日東紡氨試劑-校正液

Taiwan·Risk Class 2·NITTOBO MEDICAL CO., LTD. MEDICAL DEVELOPMENT CENTER·Registered Sep 26, 2006 – Sep 26, 2026Active

Registration details

Analysis ID: e28411eb149de981013703a9eecc5202
Customs Code: DHA00601753705

Company information

Manufacturer: NITTOBO MEDICAL CO., LTD. MEDICAL DEVELOPMENT CENTER
Manufacturer Country: Japan
Authorized Representative: TUNYEN ENTERPRISE CORPORATION

Product details

Intended Use: It is used for the determination of ammonia (NH3) in plasma correction.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1150 Calibrated Products
Import Information: import

Dates and status

Registration Date: Sep 26, 2006
Expiry Date: Sep 26, 2026

About this record

Access comprehensive regulatory information for Nitto spinning ammonia reagent-correction solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e28411eb149de981013703a9eecc5202 and manufactured by NITTOBO MEDICAL CO., LTD. MEDICAL DEVELOPMENT CENTER. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.

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