Primary Device ID | 08033390086325 |
NIH Device Record Key | 36a88aa9-f09e-4b1f-b453-093ed2dbed95 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Delta Dual Mobility System |
Version Model Number | 5566.50.401 |
Catalog Number | 5566.50.401 |
Company DUNS | 432066322 |
Company Name | LIMACORPORATE SPA |
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 |
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 | 08033390086325 [Primary] |
MBL | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-07-03 |
Device Publish Date | 2019-06-25 |
08033390086332 | Liner #M for Mobile Liner Dia. 40 mm |
08033390086325 | Mobile Liner Dia. 40 mm for Head Dia. 28 mm |
08033390020060 | Liner #L for Mobile Liner Dia. 42 mm |
08033390012447 | Mobile Liner Dia. 42 mm for Head Dia. 28 mm |