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ETHICON PHYSIOMESH OPEN Flexible Composite Mesh Device - Indonesia BPOM Medical Device Registration

ETHICON PHYSIOMESH OPEN Flexible Composite Mesh Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21602420029. The device is manufactured by JOHNSON & JOHNSON MEDICAL GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is JOHNSON AND JOHNSON INDONESIA TWO.

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BPOM Registered
Risk Class Kelas Resiko : B
ETHICON PHYSIOMESH OPEN Flexible Composite Mesh Device
Analysis ID: AKL 21602420029

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

JOHNSON AND JOHNSON INDONESIA TWO

AR Address

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

Registration Date

Mar 27, 2024

Expiry Date

May 17, 2028

Product Type

Prosthetic Surgical Equipment

Surgical mesh.

Non Electromedic Sterile

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