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INTERGRAFT Bone Chip Cancellous - Indonesia BPOM Medical Device Registration

INTERGRAFT Bone Chip Cancellous is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302812133. The device is manufactured by CELLUMED CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SKBIO NUSA MEDICA.

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BPOM Registered
Risk Class Kelas Resiko : C
INTERGRAFT Bone Chip Cancellous
Analysis ID: AKL 21302812133

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

CELLUMED CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. SKBIO NUSA MEDICA

AR Address

KOMPLEK WIJAYA GRAHA PURI BLOK G NO. 17 LT. 3 JL. WIJAYA II, KEL. PULO KEC. KEBAYORAN BARU JAKARTA SELATAN

Registration Date

Dec 05, 2022

Expiry Date

Oct 17, 2027

Product Type

Prosthetic Orthopedic Equipment

Resorbable calcium salt bone void filler device.

Non Electromedic Sterile

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