Taiwan FDA registration ccfc79e55d1729b1f4d4e2c5e56afc22

“STRENGTHEN” INFUSION STAND (Non-Sterile)

TW: “強生” 注射架 (未滅菌)

Taiwan·Risk Class 1·MD·LINET SPOL. S R. O.·Registered Apr 27, 2020 – Apr 27, 2025Expired

Registration details

Analysis ID: ccfc79e55d1729b1f4d4e2c5e56afc22
License Form: Ministry of Health Medical Device Import No. 021488
Customs Code: DHA09402148807

Company information

Manufacturer: LINET SPOL. S R. O.
Manufacturer Country: Czechia
Authorized Representative: Johnson & Johnson Medical Instruments Inc

Product details

Intended Use: Limited to the first level identification range of the "Injection Rack (J.6990)" of the Measures for the Administration of Medical Equipment.
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J6990 Injection rack
Import Information: Imported from abroad

Dates and status

Registration Date: Apr 27, 2020
Expiry Date: Apr 27, 2025

About this record

Access comprehensive regulatory information for “STRENGTHEN” INFUSION STAND (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 ccfc79e55d1729b1f4d4e2c5e56afc22 and manufactured by LINET SPOL. S R. O.. The authorized representative in Taiwan is Johnson & Johnson Medical Instruments Inc.

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.