SURGINEEDLE AUTO SUTURE Insufflation Needle - Indonesia BPOM Medical Device Registration
SURGINEEDLE AUTO SUTURE Insufflation Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801710950. The device is manufactured by COVIDIEN from United States, 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
COVIDIENCountry of Origin
United States
Authorized Representative
MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda
Registration Date
Dec 18, 2020
Expiry Date
Oct 21, 2025
Product Type
Diagnostic Gastroenterology-Urology Equipment
Endoscope and accessories.
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