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FAMILY Dr. ™ AKTIVESAFE Lancet - Indonesia BPOM Medical Device Registration

FAMILY Dr. ™ AKTIVESAFE Lancet is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603027298. The device is manufactured by BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. INDOCORE PERKASA.

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BPOM Registered
Risk Class Kelas Resiko : A
FAMILY Dr. ™ AKTIVESAFE Lancet
Analysis ID: AKL 11603027298

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. INDOCORE PERKASA

AR Address

Komplek Graha Mas Pemuda Blok AB No. 19, Jl. Pemuda RT 020 / RW 006

Registration Date

Jul 11, 2024

Expiry Date

Aug 05, 2025

Product Type

Surgical Equipment

Manual surgical instrument for general use.

Non Electromedic Sterile

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