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FREKA Tube For Feeding - Indonesia BPOM Medical Device Registration

FREKA Tube For Feeding is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805411448. The device is manufactured by CLINICO MEDICAL SP. Z.O.O from Poland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FRESENIUS KABI 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
FREKA Tube For Feeding
Analysis ID: AKL 20805411448

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Poland

Authorized Representative

PT. FRESENIUS KABI INDONESIA

AR Address

Menara Bidakara 1 Lt.19, Jl. Gatot Subroto Kav 71 - 73 Menteng Dalam, Tebet, Jakarta Selatan 12870

Registration Date

May 29, 2019

Expiry Date

Mar 13, 2024

Product Type

Therapeutic Gastroenterology-Urology Equipment

Gastrointestinal tube and accessories.

Non Electromedic Sterile

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