INTRAcel PRO - Indonesia BPOM Medical Device Registration
INTRAcel PRO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603222605. The device is manufactured by JEISYS MEDICAL INC. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is I-TECH LAFACOS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
JEISYS MEDICAL INC.Country of Origin
Korea
Authorized Representative
I-TECH LAFACOSAR Address
Gedung indra centra Blok M-N, Jl. Jendral suprapto No. 60, Kel Cempaka Putih barat , Kec. Cempaka Putih
Registration Date
Nov 02, 2022
Expiry Date
Jul 25, 2027
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
Non Radiation Electromedics
