Primary Device ID | 07613327032895 |
NIH Device Record Key | e2c4459c-096b-44c2-bc44-acc5fcecde6b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LFIT |
Version Model Number | 6260-8-336 |
Catalog Number | 6260-8-336 |
Company DUNS | 058311945 |
Company Name | Howmedica Osteonics Corp. |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Outer Diameter | 36 Millimeter |
Outer Diameter | 36 Millimeter |
Outer Diameter | 36 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613327032895 [Primary] |
LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-04-06 |
Device Publish Date | 2015-09-24 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() LFIT 86856174 not registered Dead/Abandoned |
Lblauas Group Holdings LLC 2015-12-21 |