Primary Device ID | 00840085265129 |
NIH Device Record Key | ca702f4f-64f9-477b-a1ee-0b90d9693c00 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | NBH045030 |
Catalog Number | NBH045030 |
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 |
Length | 30 Millimeter |
Outer Diameter | 4.5 Millimeter |
Length | 30 Millimeter |
Outer Diameter | 4.5 Millimeter |
Length | 30 Millimeter |
Outer Diameter | 4.5 Millimeter |
Length | 30 Millimeter |
Outer Diameter | 4.5 Millimeter |
Length | 30 Millimeter |
Outer Diameter | 4.5 Millimeter |
Length | 30 Millimeter |
Outer Diameter | 4.5 Millimeter |
Length | 30 Millimeter |
Outer Diameter | 4.5 Millimeter |
Length | 30 Millimeter |
Outer Diameter | 4.5 Millimeter |
Length | 30 Millimeter |
Outer Diameter | 4.5 Millimeter |
Length | 30 Millimeter |
Outer Diameter | 4.5 Millimeter |
Length | 30 Millimeter |
Outer Diameter | 4.5 Millimeter |
Length | 30 Millimeter |
Outer Diameter | 4.5 Millimeter |
Length | 30 Millimeter |
Outer Diameter | 4.5 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840085265129 [Primary] |
NKB | Thoracolumbosacral Pedicle Screw System |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00840085265129]
Moist Heat or Steam Sterilization
[00840085265129]
Moist Heat or Steam Sterilization
[00840085265129]
Moist Heat or Steam Sterilization
[00840085265129]
Moist Heat or Steam Sterilization
[00840085265129]
Moist Heat or Steam Sterilization
[00840085265129]
Moist Heat or Steam Sterilization
[00840085265129]
Moist Heat or Steam Sterilization
[00840085265129]
Moist Heat or Steam Sterilization
[00840085265129]
Moist Heat or Steam Sterilization
[00840085265129]
Moist Heat or Steam Sterilization
[00840085265129]
Moist Heat or Steam Sterilization
[00840085265129]
Moist Heat or Steam Sterilization
[00840085265129]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-04-19 |
Device Publish Date | 2024-04-11 |
00840085265488 - NA | 2024-04-25 CORTICAL CANCELLOUS CANNULATED SCREW |
00840085265495 - NA | 2024-04-25 CORTICAL CANCELLOUS CANNULATED SCREW |
00840085265501 - NA | 2024-04-25 CORTICAL CANCELLOUS CANNULATED SCREW |
00840085265518 - NA | 2024-04-25 CORTICAL CANCELLOUS CANNULATED SCREW |
00840085265525 - NA | 2024-04-25 CORTICAL CANCELLOUS CANNULATED SCREW |
00840085265532 - NA | 2024-04-25 CORTICAL CANCELLOUS CANNULATED SCREW |
00840085265549 - NA | 2024-04-25 CORTICAL CANCELLOUS CANNULATED SCREW |
00840085265556 - NA | 2024-04-25 CORTICAL CANCELLOUS CANNULATED SCREW |