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 21602515667. 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 PT. JOHNSON & JOHNSON NEW ZEALAND.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
JOHNSON & JOHNSON MEDICAL GMBH.Country of Origin
Germany
Authorized Representative
PT. JOHNSON & JOHNSON NEW ZEALANDAR Address
K-Link Tower Lt. 12, Jln. Jend. Gatot Subroto Kav. 59 A
Registration Date
Oct 07, 2019
Expiry Date
May 24, 2024
Product Type
Prosthetic Surgical Equipment
Surgical mesh.
Non Electromedic Sterile
ULTRAPRO ADVANCED Macroporous Partially Absorbable Mesh
ULTRAPRO Mesh
ETHICON PHYSIOMESH OPEN Flexible Composite Mesh Device
ULTRAPRO Mesh
ULTRAPRO ADVANCED Macroporous Partially Absorbable Mesh
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