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STAGEONE ™ Knee Cement Spacer Molds - Indonesia BPOM Medical Device Registration

STAGEONE ™ Knee Cement Spacer Molds is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302918761. The device is manufactured by FREUDENBERG MEDICAL, LLC from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KALMED SEJAHTERA INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
STAGEONE ™ Knee Cement Spacer Molds
Analysis ID: AKL 21302918761

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. KALMED SEJAHTERA INDONESIA

AR Address

Jl. TMII Pintu II No. 2, RT 006 RW 004,

Registration Date

Dec 30, 2019

Expiry Date

Nov 11, 2024

Product Type

Prosthetic Orthopedic Equipment

Hip joint metal/composite semi-constrained cemented prosthesis.

Non Electromedic Sterile

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