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FOLLICLE ASPIRATION SET REDUCED SINGLE LUMEN - Indonesia BPOM Medical Device Registration

FOLLICLE ASPIRATION SET REDUCED SINGLE LUMEN is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21105320062. The device is manufactured by VITROLIFE SWEDEN AB. from Sweden, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DIPA PHARMALAB INTERSAINS.

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BPOM Registered
Risk Class Kelas Resiko : B
FOLLICLE ASPIRATION SET REDUCED SINGLE LUMEN
Analysis ID: AKL 21105320062

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Sweden

Authorized Representative

DIPA PHARMALAB INTERSAINS

AR Address

Jl. Raya Kebayoran Lama No. 28, Kebayoran Lama,Jakarta Selatan, DKl Jakarta, kode pos : 12210

Registration Date

Jun 11, 2023

Expiry Date

Sep 27, 2027

Product Type

Reproductive Aids

Assisted reproduction needles.

Non Electromedic Sterile

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