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CUSTODIOL Perfusion Solution - Indonesia BPOM Medical Device Registration

CUSTODIOL Perfusion Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805112066. The device is manufactured by DR. FRANZ KOHLER CHEMIE GMBH from Germany, 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
CUSTODIOL Perfusion Solution
Analysis ID: AKL 20805112066

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. DIPA PHARMALAB INTERSAINS

AR Address

Jalan Raya Kebayoran Lama No. 28

Registration Date

Aug 19, 2019

Expiry Date

May 10, 2024

Product Type

Therapeutic Gastroenterology-Urology Equipment

Isolated kidney perfusion and transport system and accessories.

Non Electromedic Sterile

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