Primary Device ID | 00841379164371 |
NIH Device Record Key | f82dd81b-7b2f-45bb-8404-26d6a4922e3d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | N/A |
Version Model Number | BE103214B |
Catalog Number | BE103214B |
Company DUNS | 073029645 |
Company Name | HYHTE HOLDINGS, 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 | 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 | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM |
Angle | 5 degree |
Width | 10 Millimeter |
Length | 32 Millimeter |
Height | 14 Millimeter |
Angle | 5 degree |
Width | 10 Millimeter |
Length | 32 Millimeter |
Height | 14 Millimeter |
Angle | 5 degree |
Width | 10 Millimeter |
Length | 32 Millimeter |
Height | 14 Millimeter |
Angle | 5 degree |
Width | 10 Millimeter |
Length | 32 Millimeter |
Height | 14 Millimeter |
Angle | 5 degree |
Width | 10 Millimeter |
Length | 32 Millimeter |
Height | 14 Millimeter |
Angle | 5 degree |
Width | 10 Millimeter |
Length | 32 Millimeter |
Height | 14 Millimeter |
Angle | 5 degree |
Width | 10 Millimeter |
Length | 32 Millimeter |
Height | 14 Millimeter |
Angle | 5 degree |
Width | 10 Millimeter |
Length | 32 Millimeter |
Height | 14 Millimeter |
Angle | 5 degree |
Width | 10 Millimeter |
Length | 32 Millimeter |
Height | 14 Millimeter |
Angle | 5 degree |
Width | 10 Millimeter |
Length | 32 Millimeter |
Height | 14 Millimeter |
Angle | 5 degree |
Width | 10 Millimeter |
Length | 32 Millimeter |
Height | 14 Millimeter |
Angle | 5 degree |
Width | 10 Millimeter |
Length | 32 Millimeter |
Height | 14 Millimeter |
Angle | 5 degree |
Width | 10 Millimeter |
Length | 32 Millimeter |
Height | 14 Millimeter |
Angle | 5 degree |
Width | 10 Millimeter |
Length | 32 Millimeter |
Height | 14 Millimeter |
Angle | 5 degree |
Width | 10 Millimeter |
Length | 32 Millimeter |
Height | 14 Millimeter |
Angle | 5 degree |
Width | 10 Millimeter |
Length | 32 Millimeter |
Height | 14 Millimeter |
Angle | 5 degree |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841379164371 [Primary] |
MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00841379164371]
Moist Heat or Steam Sterilization
[00841379164371]
Moist Heat or Steam Sterilization
[00841379164371]
Moist Heat or Steam Sterilization
[00841379164371]
Moist Heat or Steam Sterilization
[00841379164371]
Moist Heat or Steam Sterilization
[00841379164371]
Moist Heat or Steam Sterilization
[00841379164371]
Moist Heat or Steam Sterilization
[00841379164371]
Moist Heat or Steam Sterilization
[00841379164371]
Moist Heat or Steam Sterilization
[00841379164371]
Moist Heat or Steam Sterilization
[00841379164371]
Moist Heat or Steam Sterilization
[00841379164371]
Moist Heat or Steam Sterilization
[00841379164371]
Moist Heat or Steam Sterilization
[00841379164371]
Moist Heat or Steam Sterilization
[00841379164371]
Moist Heat or Steam Sterilization
[00841379164371]
Moist Heat or Steam Sterilization
[00841379164371]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-02-24 |
Device Publish Date | 2018-02-16 |
00841379164388 | TLIF SPACER |
00841379164371 | TLIF SPACER |
00841379164364 | TLIF SPACER |
00841379164357 | TLIF SPACER |
00841379164340 | TLIF SPACER |
00841379164333 | TLIF SPACER |
00841379164326 | TLIF SPACER |
00841379164319 | TLIF SPACER |
00841379164302 | TLIF SPACER |
00841379164296 | TLIF SPACER |
00841379164289 | TLIF SPACER |
00841379164272 | TLIF SPACER |
00841379164265 | TLIF SPACER |
00841379164258 | TLIF SPACER |
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00841379164197 | TLIF SPACER |
00841379164180 | TLIF SPACER |
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00841379164166 | TLIF SPACER |
00841379164159 | TLIF SPACER |
00841379164142 | TLIF SPACER |
00841379164135 | TLIF SPACER |
00841379164128 | TLIF SPACER |
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00841379164098 | TLIF SPACER |
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00841379164074 | TLIF SPACER |
00841379164067 | TLIF SPACER |
00841379164050 | TLIF SPACER |
00841379164043 | TLIF SPACER |
00841379164036 | TLIF SPACER |
00841379139898 | OTLIF SPACER, PEEK, 10MMX22MMX08MMX5°, NON-STERILE |
00841379100614 | OTLIF SPACER, PEEK, 10MMX22MMX14MMX5°, NON-STERILE |
00841379100607 | OTLIF SPACER, PEEK, 10MMX22MMX13MMX5°, NON-STERILE |
00841379100584 | OTLIF SPACER, PEEK, 10MMX22MMX11MMX5°, NON-STERILE |
00841379100577 | OTLIF SPACER, PEEK, 10MMX22MMX10MMX5°, NON-STERILE |
00841379100560 | OTLIF SPACER, PEEK, 10MMX22MMX09MMX5°, NON-STERILE |
00841379100553 | OTLIF SPACER, PEEK, 10MMX22MMX07MMX5°, NON-STERILE |
00841379100546 | TLIF SPACER |
00841379100539 | TLIF SPACER |
00841379100522 | TLIF SPACER |
00841379100515 | TLIF SPACER |
00841379100508 | TLIF SPACER |
00841379100492 | TLIF SPACER |
00841379100485 | TLIF SPACER |