Primary Device ID | M572RBK1011112021 |
NIH Device Record Key | a5b58470-c6e2-4f9a-a081-04d7bbcf0aaf |
Commercial Distribution Discontinuation | 2022-08-15 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | iDuo® Femoral Kit |
Version Model Number | RBK101111202 |
Catalog Number | RBK1011112 |
Company DUNS | 808821883 |
Company Name | Conformis, Inc. |
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 | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | false |
Serial Number | true |
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 | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com |
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 |
---|---|
HIBCC | M572RBK1011112021 [Primary] |
OOG | Knee Arthroplasty Implantation System |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2022-08-16 |
Device Publish Date | 2015-10-26 |
M572RBK1011112021 | N/A |
M572RBK1011112011 | RBK101111201 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
IDUO 85794905 not registered Dead/Abandoned |
i do it sarl 2012-12-05 |
IDUO 85518103 4270942 Live/Registered |
Liang, Hsien-Rong 2012-01-17 |
IDUO 78652189 not registered Dead/Abandoned |
Liang, Hsien-Rong 2005-06-16 |
IDUO 77200574 3459154 Dead/Cancelled |
ConforMIS, Inc. 2007-06-07 |
IDUO 77087559 not registered Dead/Abandoned |
I DO IT SPRLU 2007-01-22 |