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STANDARD E TB-Feron Tubes 300 - Indonesia BPOM Medical Device Registration

STANDARD E TB-Feron Tubes 300 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101221318. The device is manufactured by SD BIOSENSOR INC. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. STANDARD BIOSENSOR INDONESIA.

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
STANDARD E TB-Feron Tubes 300
Analysis ID: AKL 20101221318

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SD BIOSENSOR INC.

Country of Origin

Korea

Authorized Representative

PT. STANDARD BIOSENSOR INDONESIA

AR Address

L'AVENUE BUILDING UNIT C, LT. 21, JL. RAYA PASAR MINGGU KAV. 16

Registration Date

Jul 31, 2024

Expiry Date

Jan 18, 2029

Product Type

Clinical Chemistry Test System

Blood specimen collection device

Invitro Diagnostics

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