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HOLLISTER New Image 2-Piece Urostomy Pouch - Indonesia BPOM Medical Device Registration

HOLLISTER New Image 2-Piece Urostomy Pouch is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10805027357. The device is manufactured by HOLLISTER INCORPORATED from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. LABORA MANDIRI INDO PRATAMA.

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
HOLLISTER New Image 2-Piece Urostomy Pouch
Analysis ID: AKL 10805027357

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United States

Authorized Representative

PT. LABORA MANDIRI INDO PRATAMA

AR Address

Jl. C. Simanjuntak No. 47

Registration Date

Nov 30, 2022

Expiry Date

Dec 31, 2025

Product Type

Therapeutic Gastroenterology-Urology Equipment

Ostomy pouch and accessories.

Non Electromedic Non Sterile

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