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ETHICON Hernia Kit - Indonesia BPOM Medical Device Registration

ETHICON Hernia Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603802507. The device is manufactured by JOHNSON & JOHNSON PRIVATE LIMITED from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. JOHNSON & JOHNSON NEW ZEALAND.

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
ETHICON Hernia Kit
Analysis ID: AKL 21603802507

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. JOHNSON & JOHNSON NEW ZEALAND

AR Address

K-Link Tower Lt. 12, Jln. Jend. Gatot Subroto Kav. 59 A

Registration Date

Feb 04, 2021

Expiry Date

Jul 30, 2025

Product Type

Prosthetic Surgical Equipment

Surgical mesh.

Non Electromedic Sterile

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