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DUALPOR Collagen Putty - Indonesia BPOM Medical Device Registration

DUALPOR Collagen Putty is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302220420. The device is manufactured by OSSGEN 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
DUALPOR Collagen Putty
Analysis ID: AKL 21302220420

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

OSSGEN 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

Nov 16, 2022

Expiry Date

Aug 10, 2027

Product Type

Prosthetic Orthopedic Equipment

Resorbable calcium salt bone void filler device.

Non Electromedic Sterile

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