Home GUDID 00841523101153 Kyocera Medical Technologies, Inc.
Primary DI 00841523101153
Brand Kyocera Medical Technologies, Inc.
Company KYOCERA MEDICAL TECHNOLOGIES, INC.
Model A 200
Catalog number 1201-132-320
Device description L CR E-MAXTM Vitamin E Ultracongruent Tibial Insert Sz B 20mm
Published 2015-10-28
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Sterile true
Single use true Product Codes# Code, Name table Code Name JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer OIY Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer Orthopedic 2 OIY Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00841523101153 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00841523101153 00841523101153 841523101153 0841523101153
GMDN Terms# Term, Definition table Term Definition Cruciate-retaining total knee prosthesis A sterile implantable artificial substitute for a knee joint typically designed to replace all the articulating surfaces of the damaged/degenerative (e.g., arthritic) joint [total knee arthroplasty (TKA)]; it is designed to be implanted with retention of the posterior cruciate ligament. It typically includes femoral, tibial, and patellar components that articulate and with parts made of metal, ceramic, and/or polyethylene (PE). The device may be implanted with or without bone cement and is typically used in cases where bone stock is good and supporting ligaments provide adequate stability.
Regulatory Flags# DUNS number 116995646 Device count 1 Lot or batch true Expiration date on label true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00841523183944 Kyocera Medical Technologies, Inc. Initia T3 3535-851-012 2026-08-21 00841523183999 Kyocera Medical Technologies, Inc. Tesera-k ALIF 2167-001-511 2026-08-21 00841523184002 Kyocera Medical Technologies, Inc. Tesera-k ALIF 2167-001-513 2026-08-21 00841523184019 Kyocera Medical Technologies, Inc. Tesera-k ALIF 2167-001-515 2026-08-21 00841523184026 Kyocera Medical Technologies, Inc. Tesera-k ALIF 2167-001-517 2026-08-21 00841523184033 Kyocera Medical Technologies, Inc. Tesera-k ALIF 2167-001-519 2026-08-21 00841523184040 Kyocera Medical Technologies, Inc. Tesera-k ALIF 2167-001-521 2026-08-21 00841523185337 Kyocera Medical Technologies, Inc. Tesera-K-SC 3061-011-016 2026-08-21 00841523183081 Kyocera Medical Technologies, Inc. Tesera-K XL 2173-001-003 2026-08-07 00841523183746 Kyocera Medical Technologies, Inc. Tesera-K XL 3073-005-000 2026-08-07 00841523185030 Kyocera Medical Technologies, Inc. Tesera-K XL 2173-018-108 2026-08-07 00841523185047 Kyocera Medical Technologies, Inc. Tesera-K XL 2173-018-110 2026-08-07 00841523185054 Kyocera Medical Technologies, Inc. Tesera-K XL 2173-018-112 2026-08-07 00841523185061 Kyocera Medical Technologies, Inc. Tesera-K XL 2173-018-114 2026-08-07 00841523185078 Kyocera Medical Technologies, Inc. Tesera-K XL 2173-018-116 2026-08-07 00841523185092 Kyocera Medical Technologies, Inc. Tesera-K XL 2173-018-210 2026-08-07 00841523185108 Kyocera Medical Technologies, Inc. Tesera-K XL 2173-018-212 2026-08-07 00841523185139 Kyocera Medical Technologies, Inc. Tesera-K XL 2173-022-108 2026-08-07 00841523185146 Kyocera Medical Technologies, Inc. Tesera-K XL 2173-022-110 2026-08-07 00841523185153 Kyocera Medical Technologies, Inc. Tesera-K XL 2173-022-112 2026-08-07
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