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NEOMEDICA NEO RINSE E - Indonesia BPOM Medical Device Registration

NEOMEDICA NEO RINSE E is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204320505. The device is manufactured by NEOMEDICA DOO from Serbia, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ELGA TAMA.

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Risk Class Kelas Resiko : A
NEOMEDICA NEO RINSE E
Analysis ID: AKL 10204320505

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

NEOMEDICA DOO

Country of Origin

Serbia

Authorized Representative

PT. ELGA TAMA

AR Address

JL. RASAMALA RAYA NO. 12 D RT. 006 RW. 003 KELURAHAN JATIPULO, KECAMATAN PALMERAH

Registration Date

May 27, 2024

Expiry Date

Mar 29, 2027

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

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