Primary Device ID | 00851599007785 |
NIH Device Record Key | 02546068-6657-4987-8d9b-ea618a5b0523 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | O Plate, 6 Holes, Provisional |
Version Model Number | 215.114.06 |
Company DUNS | 063554875 |
Company Name | JACE MEDICAL, LLC |
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 | false |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00851599007785 [Primary] |
PBF | Orthopaedic Surgical Planning And Instrument Guides |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00851599007785]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-02-07 |
Device Publish Date | 2018-01-26 |
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