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FEMITIA FEMIJECT DUO - Indonesia BPOM Medical Device Registration

FEMITIA FEMIJECT DUO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902221416. The device is manufactured by WUXI YUSHOU MEDICAL APPLIANCES CO LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TUNGGAL SILA FARMA.

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BPOM Registered
Risk Class Kelas Resiko : B
FEMITIA FEMIJECT DUO
Analysis ID: AKL 20902221416

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. TUNGGAL SILA FARMA

AR Address

Jl. Jend. A. Yani No. 2

Registration Date

Dec 16, 2022

Expiry Date

Dec 14, 2025

Product Type

Therapeutic General and Individual Hospital Equipment

Piston syringe.

Non Electromedic Sterile

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