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VITROLIFE Holding Pipette - Indonesia BPOM Medical Device Registration

VITROLIFE Holding Pipette is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21105320091. The device is manufactured by VITROLIFE INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DIPA PHARMALAB INTERSAINS.

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BPOM Registered
Risk Class Kelas Resiko : B
VITROLIFE Holding Pipette
Analysis ID: AKL 21105320091

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

VITROLIFE INC

Country of Origin

United States

Authorized Representative

PT. DIPA PHARMALAB INTERSAINS

AR Address

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

Registration Date

Sep 08, 2023

Expiry Date

Sep 27, 2027

Product Type

Reproductive Aids

Assisted reproduction micromanipulators and microinjectors.

Non Electromedic Sterile

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