ENDOLOOP Ligature made with PDS II (Polydioxanone) Suture - Indonesia BPOM Medical Device Registration
ENDOLOOP Ligature made with PDS II (Polydioxanone) Suture is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603420921. The device is manufactured by JOHNSON & JOHNSON OF BRAZIL IND. COM. OF PROD. P/HEALTH LTDA. from Brazil, and is classified as Risk Class Kelas Resiko : C. 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.
Risk Classification
Product Class
Kelas : 2
Country of Origin
Brazil
Authorized Representative
JOHNSON AND JOHNSON INDONESIA TWOAR Address
K-Link Tower, Lt. 15, Jl. Jend. Gatot Subroto kav. 59A.
Registration Date
Apr 29, 2024
Expiry Date
Feb 27, 2029
Product Type
Surgical Equipment
Absorbable polydioxanone surgical suture.
Non Electromedic Sterile
ECHELON 3000 60mm Stapler
NYPRO HEALTHCARE BAJA, INC.
ECHELON 3000 60mm Stapler
NYPRO HEALTHCARE BAJA, INC.
ECHELON 3000 60mm Stapler
NYPRO HEALTHCARE BAJA, INC.
ECHELON 3000 45mm Stapler
NYPRO HEALTHCARE BAJA, INC.
ECHELON 3000 45mm Stapler
NYPRO HEALTHCARE BAJA, INC.
ECHELON 3000 45mm Stapler
NYPRO HEALTHCARE BAJA, INC.
ATTUNE All Poly Tibia
DEPUY ORTHOPAEDICS, INC.
HARMONIC 700 Shears
NPA DE MEXICO S, DE R.L DE C.V.
CORAIL HIP SYSTEM - Corail Revision Femoral Stem
VIANT CHAUMONT SAS
STRATAFIX Spiral PDS Plus Knotless Tissue Control Device (Bi-Directional)
ETHICON, LLC.