VersaOne™ Fascial Closure System Reusable Suture Passer - Indonesia BPOM Medical Device Registration
VersaOne™ Fascial Closure System Reusable Suture Passer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801021772. The device is manufactured by ACKERMANN INSTRUMENTE GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MEDTRONIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ACKERMANN INSTRUMENTE GMBHCountry of Origin
Germany
Authorized Representative
MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda
Registration Date
Apr 07, 2020
Expiry Date
Mar 12, 2025
Product Type
Diagnostic Gastroenterology-Urology Equipment
Endoscope and accessories
Non Electromedic Non Sterile
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