Taiwan FDA registration 88b0ed5ce8f26bfa7ff94728a5ec8135

"Pulliton" diagnostic sampling swab (sterilized)

TW: “普立頓”診斷採樣拭子 (滅菌)

Taiwan·Risk Class 1·PURITAN MEDICAL PRODUCTS COMPANY LLC·Registered Apr 18, 2014 – Apr 18, 2029Active

Registration details

Analysis ID: 88b0ed5ce8f26bfa7ff94728a5ec8135
Customs Code: DHA09401406807

Company information

Manufacturer: PURITAN MEDICAL PRODUCTS COMPANY LLC
Manufacturer Country: United States
Authorized Representative: ICON INC.

Product details

Intended Use: Limited to the classification and grading management measures for medical equipment "Microbial Sample Collection and Delivery Equipment (C.2900)" the first level identification range.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.2900 Microbial sample collection and delivery equipment
Import Information: QMS/QSD;; 輸入

Dates and status

Registration Date: Apr 18, 2014
Expiry Date: Apr 18, 2029

About this record

Access comprehensive regulatory information for "Pulliton" diagnostic sampling swab (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 88b0ed5ce8f26bfa7ff94728a5ec8135 and manufactured by PURITAN MEDICAL PRODUCTS COMPANY LLC. The authorized representative in Taiwan is ICON INC..

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