ZENER Intervertebral Fusion Cage - Indonesia BPOM Medical Device Registration
ZENER Intervertebral Fusion Cage is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302321039. The device is manufactured by ZENER MEDTEC (CHANGZHOU) CO.,LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ADHIRA MEDIKA PERSADA INTERNATIONAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ZENER MEDTEC (CHANGZHOU) CO.,LTDCountry of Origin
China
Authorized Representative
ADHIRA MEDIKA PERSADA INTERNATIONALAR Address
Ruko Paramount Sparks B No. 17, Jl. Raya Kelapa Dua Gading Serpong
Registration Date
Dec 15, 2023
Expiry Date
Aug 08, 2027
Product Type
Prosthetic Orthopedic Equipment
Intervertebral body fusion device
Non Electromedic Sterile
