AZE130045

GUDID 00841379165606

MIS BONE TAP,

HYHTE HOLDINGS, INC.

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Primary Device ID00841379165606
NIH Device Record Key6b18021b-67ce-4c95-94ac-7a85363028f2
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberAZE130045
Catalog NumberAZE130045
Company DUNS073029645
Company NameHYHTE HOLDINGS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM

Device Dimensions

Outer Diameter4.5 Millimeter
Outer Diameter4.5 Millimeter
Outer Diameter4.5 Millimeter
Outer Diameter4.5 Millimeter
Outer Diameter4.5 Millimeter
Outer Diameter4.5 Millimeter
Outer Diameter4.5 Millimeter
Outer Diameter4.5 Millimeter
Outer Diameter4.5 Millimeter
Outer Diameter4.5 Millimeter
Outer Diameter4.5 Millimeter
Outer Diameter4.5 Millimeter
Outer Diameter4.5 Millimeter
Outer Diameter4.5 Millimeter
Outer Diameter4.5 Millimeter
Outer Diameter4.5 Millimeter
Outer Diameter4.5 Millimeter
Outer Diameter4.5 Millimeter
Outer Diameter4.5 Millimeter
Outer Diameter4.5 Millimeter
Outer Diameter4.5 Millimeter
Outer Diameter4.5 Millimeter
Outer Diameter4.5 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100841379165606 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00841379165606]

Moist Heat or Steam Sterilization


[00841379165606]

Moist Heat or Steam Sterilization


[00841379165606]

Moist Heat or Steam Sterilization


[00841379165606]

Moist Heat or Steam Sterilization


[00841379165606]

Moist Heat or Steam Sterilization


[00841379165606]

Moist Heat or Steam Sterilization


[00841379165606]

Moist Heat or Steam Sterilization


[00841379165606]

Moist Heat or Steam Sterilization


[00841379165606]

Moist Heat or Steam Sterilization


[00841379165606]

Moist Heat or Steam Sterilization


[00841379165606]

Moist Heat or Steam Sterilization


[00841379165606]

Moist Heat or Steam Sterilization


[00841379165606]

Moist Heat or Steam Sterilization


[00841379165606]

Moist Heat or Steam Sterilization


[00841379165606]

Moist Heat or Steam Sterilization


[00841379165606]

Moist Heat or Steam Sterilization


[00841379165606]

Moist Heat or Steam Sterilization


[00841379165606]

Moist Heat or Steam Sterilization


[00841379165606]

Moist Heat or Steam Sterilization


[00841379165606]

Moist Heat or Steam Sterilization


[00841379165606]

Moist Heat or Steam Sterilization


[00841379165606]

Moist Heat or Steam Sterilization


[00841379165606]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-06-10
Device Publish Date2021-06-02

Devices Manufactured by HYHTE HOLDINGS, INC.

00840085265488 - NA2024-04-25 CORTICAL CANCELLOUS CANNULATED SCREW
00840085265495 - NA2024-04-25 CORTICAL CANCELLOUS CANNULATED SCREW
00840085265501 - NA2024-04-25 CORTICAL CANCELLOUS CANNULATED SCREW
00840085265518 - NA2024-04-25 CORTICAL CANCELLOUS CANNULATED SCREW
00840085265525 - NA2024-04-25 CORTICAL CANCELLOUS CANNULATED SCREW
00840085265532 - NA2024-04-25 CORTICAL CANCELLOUS CANNULATED SCREW
00840085265549 - NA2024-04-25 CORTICAL CANCELLOUS CANNULATED SCREW
00840085265556 - NA2024-04-25 CORTICAL CANCELLOUS CANNULATED SCREW

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