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ReBorn Essence Venus Cervical Intervertebral Cage - Indonesia BPOM Medical Device Registration

ReBorn Essence Venus Cervical Intervertebral Cage is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302420258. The device is manufactured by BAUI BIOTECH CO., LTD. from Taiwan (China), and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ARJAYA LANGGENG MEDIKA.

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Risk Class Kelas Resiko : C
ReBorn Essence Venus Cervical Intervertebral Cage
Analysis ID: AKL 21302420258

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

ARJAYA LANGGENG MEDIKA

AR Address

GRAHA SIMATUPANG TOWER 2C, LANTAI 4. JL. TB. SIMATUPANG KAV. 38 Kode Pos: 12540

Registration Date

Jul 31, 2024

Expiry Date

Jan 29, 2029

Product Type

Prosthetic Orthopedic Equipment

Intervertebral body fusion device

Non Electromedic Sterile

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