Taiwan FDA registration 5f225d48f378ea220bb13157a9b056df

"Fore" safe lancet (sterilized)

TW: “福爾” 安全採血針(滅菌)

Taiwan·Risk Class 1·BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD.·Registered Feb 18, 2016 – Feb 18, 2026Expired

Registration details

Analysis ID: 5f225d48f378ea220bb13157a9b056df
Customs Code: DHA09600263809

Company information

Manufacturer: BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD.
Manufacturer Country: China
Authorized Representative: TAIDOC TECHNOLOGY CORPORATION

Product details

Intended Use: Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: QMS/QSD;; Input;; Chinese goods

Dates and status

Registration Date: Feb 18, 2016
Expiry Date: Feb 18, 2026

About this record

Access comprehensive regulatory information for "Fore" safe lancet (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5f225d48f378ea220bb13157a9b056df and manufactured by BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD.. The authorized representative in Taiwan is TAIDOC TECHNOLOGY CORPORATION.

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.