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OXMED ZenSiv Colostomy Bag - Indonesia BPOM Medical Device Registration

OXMED ZenSiv Colostomy Bag is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10805126123. The device is manufactured by OXMED INTERNATIONAL GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is ENDO 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 : A
OXMED ZenSiv Colostomy Bag
Analysis ID: AKL 10805126123

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

ENDO INDONESIA

AR Address

Jl. Raya Menganti 14

Registration Date

Oct 17, 2021

Expiry Date

Apr 19, 2026

Product Type

Therapeutic Gastroenterology-Urology Equipment

Ostomy pouch and accessories.

Non Electromedic Non Sterile

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