Primary Device ID | 00848665019698 |
NIH Device Record Key | da53c1ce-4ccf-484c-b01b-d45e9efb3a6b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CORTICAL SCREW 3.5mm x 26.0mm |
Version Model Number | 8010-260 |
Company DUNS | 117858154 |
Company Name | ADVANCED ORTHOPEDIC SOLUTIONS 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 | 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 Issuing Agency | Device ID |
---|---|
GS1 | 00848665019698 [Primary] |
HSB | Rod, Fixation, Intramedullary And Accessories |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00848665019698]
Moist Heat or Steam Sterilization
[00848665019698]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-12-22 |
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