Primary Device ID | 00889797103978 |
NIH Device Record Key | 0c1f9cca-3827-47f5-b444-8227caa5488e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PROstep MIS |
Version Model Number | 57S05052 |
Catalog Number | 57S05052 |
Company DUNS | 807201207 |
Company Name | WRIGHT MEDICAL TECHNOLOGY, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com | |
Phone | +1(800)238-7117 |
customerservice@wmt.com |
Outer Diameter | 5 Millimeter |
Length | 52 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 52 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 52 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 52 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 52 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 52 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 52 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 52 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 52 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 52 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 52 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 52 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 52 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 52 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 52 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 52 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 52 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 52 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889797103978 [Primary] |
HWC | Screw, fixation, bone |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-08-04 |
Device Publish Date | 2023-07-27 |
00889797104050 | Chamfer Screw |
00889797104043 | Chamfer Screw |
00889797104012 | Chamfer Screw |
00889797103992 | Chamfer Screw |
00889797103985 | Chamfer Screw |
00889797103978 | Chamfer Screw |
00889797103954 | Chamfer Screw |
00889797103916 | Chamfer Screw |
00889797103879 | Chamfer Screw |
00889797103862 | Chamfer Screw |
00889797103923 | Chamfer Screw |