Primary Device ID | 10886705020720 |
NIH Device Record Key | fb760c21-4f59-41ce-aa20-99f6620d9d1f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BRISTOW LATARJET |
Version Model Number | 285142 |
Catalog Number | 285142 |
Company DUNS | 190572854 |
Company Name | DEPUY MITEK, LLC |
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 | 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 |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10886705020720 [Primary] |
HWC | Screw, fixation, bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[10886705020720]
Moist Heat or Steam Sterilization
[10886705020720]
Moist Heat or Steam Sterilization
[10886705020720]
Moist Heat or Steam Sterilization
[10886705020720]
Moist Heat or Steam Sterilization
[10886705020720]
Moist Heat or Steam Sterilization
[10886705020720]
Moist Heat or Steam Sterilization
[10886705020720]
Moist Heat or Steam Sterilization
[10886705020720]
Moist Heat or Steam Sterilization
[10886705020720]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2021-08-30 |
Device Publish Date | 2015-09-01 |
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