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ULTRAPRO PLUG - Indonesia BPOM Medical Device Registration

ULTRAPRO PLUG is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21602420030. The device is manufactured by JOHNSON & JOHNSON INTERNATIONAL from Belgium, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is JOHNSON AND JOHNSON INDONESIA TWO.

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
ULTRAPRO PLUG
Analysis ID: AKL 21602420030

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Belgium

Authorized Representative

JOHNSON AND JOHNSON INDONESIA TWO

AR Address

K-Link Tower, Lt. 15, Jl. Jend. Gatot Subroto kav. 59A.

Registration Date

Mar 28, 2024

Expiry Date

May 17, 2028

Product Type

Prosthetic Surgical Equipment

Surgical mesh.

Non Electromedic Sterile

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