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FESCO Stomach Tube - Indonesia BPOM Medical Device Registration

FESCO Stomach Tube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805513957. The device is manufactured by WELL LEAD MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FESCO 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
FESCO Stomach Tube
Analysis ID: AKL 20805513957

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. FESCO INDONESIA

AR Address

KOMP. RUKO MEGA GROSIR CEMPAKA MAS BLOK E 1, NO. 17, JL.LETJEN SOEPRAPTO , JAKARTA PUSAT, 10640

Registration Date

Jan 15, 2021

Expiry Date

Oct 05, 2025

Product Type

Therapeutic Gastroenterology-Urology Equipment

Gastrointestinal tube and accessories.

Non Electromedic Sterile

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