Primary Device ID | 09340499017761 |
NIH Device Record Key | 07ff7f78-b9f7-411e-b295-c7d51ce6bdb4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RBK Patello Femoral |
Version Model Number | GO-6000-1PFR-01 |
Catalog Number | GO-6000-1PFR-01 |
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 | true |
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 | |
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 Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 09340499017761 [Primary] |
KRR | Prosthesis, Knee, Patello/Femoral, 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 | 2019-12-11 |
Device Publish Date | 2016-03-09 |
09340499022710 | RBK Patello Femoral Size 4 Right |
09340499022703 | RBK Patello Femoral Size 4 Left |
09340499017808 | RBK Patello Femoral Size 3 Right |
09340499017792 | RBK Patello Femoral Size 3 Left |
09340499017785 | RBK Patello Femoral Size 2 Right |
09340499017778 | RBK Patello Femoral Size 2 Left |
09340499017761 | RBK Patello Femoral Size 1 Right |
09340499017754 | RBK Patello Femoral Size 1 Left |
09340499017747 | RBK Patello Femoral Size 0 Right |
09340499017730 | RBK Patello Femoral Size 0 Left |
09340499004662 | RBK Patella 40mm |
09340499004655 | RBK Patella 36mm |
09340499004648 | RBK Patella 32mm |
09340499004631 | RBK Patella 28mm |