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COMBOSTIK R-600S and Accessories - Indonesia BPOM Medical Device Registration

COMBOSTIK R-600S and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102220229. The device is manufactured by DFI CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SABA INDOMEDIKA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
COMBOSTIK R-600S and Accessories
Analysis ID: AKL 20102220229

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

DFI CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. SABA INDOMEDIKA

AR Address

Ruko Kedoya Elok Plaza DB-33 Jl. Panjang No.7-9

Registration Date

Aug 19, 2024

Expiry Date

Jul 11, 2029

Product Type

Clinical Laboratory Equipment

Automated urinalysis system.

Invitro Diagnostics

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