Primary Device ID | 10812269021132 |
NIH Device Record Key | c2670801-4538-4fa0-bb19-356b6e9e72ed |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PHLP Drill Guide Block, Left |
Version Model Number | MDS130904L |
Catalog Number | MDS130904L |
Company DUNS | 078703080 |
Company Name | MIAMI DEVICE SOLUTIONS 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 | true |
OTC Over-The-Counter | false |
Phone | 786-422-1400 |
customerservice@miamidevicesolutions.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10812269021132 [Primary] |
HRS | Plate, Fixation, Bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[10812269021132]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-03-05 |
Device Publish Date | 2020-02-26 |
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