NEXGEN LCCK System - Indonesia BPOM Medical Device Registration
NEXGEN LCCK System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302918862. The device is manufactured by ZIMMER INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KALMED SEJAHTERA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ZIMMER INC.Country of Origin
United States
Authorized Representative
PT. KALMED SEJAHTERA INDONESIAAR Address
JL.TAMAN MINI PINTU 2 NO. 2, RT. 006 RW. 004
Registration Date
Dec 10, 2024
Expiry Date
Dec 08, 2026
Product Type
Prosthetic Orthopedic Equipment
Knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis.
Non Electromedic Sterile
ZIMMER Persona Instruments 2
ZIMMER Trabecular Metal Acetabular Revision System (TMARS) Instruments
HGP II Bone Screws
NEXGEN Complete Knee Solution, Rotating Hinge Knee (RHK) - Articular Surface, Tibial, Femoral Components
ZIMMER BIOMET 12/14 Head Trials
ZIMMER Persona Instruments
CABLE READY Cable Grip System
NEXGEN Rotating Hinge Knee (RHK) Instruments
ZIMMER Cable Ready Instruments Set
NEXGEN LCCK Instruments
ZIMMER Sterile Disposable Tourniquet Cuff
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ZIMMER Trabecular Metal Acetabular Revision System (TMARS) Instruments
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NEXGEN Complete Knee Solution, Rotating Hinge Knee (RHK) - Articular Surface, Tibial, Femoral Components
ZIMMER INC.
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ZIMMER CAS