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VITROLIFE Serological Pipette - Indonesia BPOM Medical Device Registration

VITROLIFE Serological Pipette is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21105024255. The device is manufactured by HERTART APS. from Sweden, 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 Serological Pipette
Analysis ID: AKL 21105024255

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

HERTART APS.

Country of Origin

Sweden

Authorized Representative

PT. DIPA PHARMALAB INTERSAINS

AR Address

Jalan Raya Kebayoran Lama No. 28

Registration Date

Aug 01, 2020

Expiry Date

May 18, 2025

Product Type

Reproductive Aids

Assisted reproduction labware.

Invitro Diagnostics

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