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ICSI Pipette Micromanipulation Pipettes - Indonesia BPOM Medical Device Registration

ICSI Pipette Micromanipulation Pipettes is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21105818554. 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 DIPA PHARMALAB INTERSAINS.

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BPOM Registered
Risk Class Kelas Resiko : B
ICSI Pipette Micromanipulation Pipettes
Analysis ID: AKL 21105818554

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

VITROLIFE INC.

Country of Origin

United States

Authorized Representative

DIPA PHARMALAB INTERSAINS

AR Address

Jalan Raya Kebayoran Lama No. 28

Registration Date

Jan 20, 2021

Expiry Date

Nov 13, 2025

Product Type

Reproductive Aids

Assisted reproduction micropipette fabrication instruments.

Invitro Diagnostics

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