Primary Device ID | 00854629006284 |
NIH Device Record Key | d7d07340-3f27-4733-8892-b15288c5bd39 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PunchTac 5.5 Anchor PEEK |
Version Model Number | DFX0036A |
Catalog Number | DFX0036A |
Company DUNS | 079471560 |
Company Name | DUNAMIS MEDICAL, LLC |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
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 |
Phone | 877.454.2186 |
info@dunamismedical.com | |
Phone | 877.454.2186 |
info@dunamismedical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00854629006277 [Primary] |
GS1 | 00854629006284 [Package] Contains: 00854629006277 Package: [5 Units] In Commercial Distribution |
MBI | Fastener, Fixation, Nondegradable, Soft Tissue |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-04-12 |
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