Primary Device ID | 09340499005546 |
NIH Device Record Key | 4bfbac33-4ed1-4a92-857b-57cfde32e676 |
Commercial Distribution Discontinuation | 2021-07-14 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | GRU Femur |
Version Model Number | GRU-RM/LL-5F-C |
Catalog Number | GRU-RM/LL-5F-C |
Company DUNS | 752039982 |
Company Name | GLOBAL MANUFACTURING TECHNOLOGY PTY LIMITED |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +6128870100 |
info@globalortho.com.au | |
Phone | +6128870100 |
info@globalortho.com.au | |
Phone | +6128870100 |
info@globalortho.com.au | |
Phone | +6128870100 |
info@globalortho.com.au | |
Phone | +6128870100 |
info@globalortho.com.au | |
Phone | +6128870100 |
info@globalortho.com.au | |
Phone | +6128870100 |
info@globalortho.com.au | |
Phone | +6128870100 |
info@globalortho.com.au | |
Phone | +6128870100 |
info@globalortho.com.au | |
Phone | +6128870100 |
info@globalortho.com.au | |
Phone | +6128870100 |
info@globalortho.com.au | |
Phone | +6128870100 |
info@globalortho.com.au | |
Phone | +6128870100 |
info@globalortho.com.au | |
Phone | +6128870100 |
info@globalortho.com.au | |
Phone | +6128870100 |
info@globalortho.com.au | |
Phone | +6128870100 |
info@globalortho.com.au | |
Phone | +6128870100 |
info@globalortho.com.au |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 09340499005546 [Primary] |
HRY | Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2021-07-14 |
Device Publish Date | 2016-03-09 |
09340499005546 | GRU Femur RMLL Size 5 |
09340499005539 | GRU Femur RMLL Size 4 |
09340499005522 | GRU Femur RMLL Size 3 |
09340499005515 | GRU Femur RMLL Size 2 |
09340499005508 | GRU Femur RMLL Size 1 |
09340499005492 | GRU Femur RMLL Size 0 |
09340499005485 | GRU Femur RLLM Size 5 |
09340499005478 | GRU Femur RLLM Size 4 |
09340499005461 | GRU Femur RLLM Size 3 |
09340499005454 | GRU Femur RLLM Size 2 |
09340499005447 | GRU Femur RLLM Size 1 |
09340499005430 | GRU Femur RLLM Size 0 |