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BECKMAN COULTER Access Progesterone II - Indonesia BPOM Medical Device Registration

BECKMAN COULTER Access Progesterone II is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101520128. The device is manufactured by BECKMAN COULTER ,INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DHH TRADING INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
BECKMAN COULTER Access Progesterone II
Analysis ID: AKL 20101520128

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. DHH TRADING INDONESIA

AR Address

Revenue Tower 19F, Jl. Jenderal Sudirman No. 52-53, Prov. DKI Jakarta, Kota Adm. Jakarta Selatan, Kec Kebayoran Baru, Kel Senayan

Registration Date

Jan 20, 2025

Expiry Date

Mar 28, 2029

Product Type

Clinical Chemistry Test System

Progesterone test system (kit & cair)

Invitro Diagnostics

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