AZA026500

GUDID 00841379106210

GUIDE WIRE, SHARP TIP, 1.4MM X XXXMM, NITINOL

HYHTE HOLDINGS, INC.

Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual
Primary Device ID00841379106210
NIH Device Record Key47a19aa5-bbd0-4a90-8b72-b58369d6ba3e
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberAZA026500
Catalog NumberAZA026500
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

Device Dimensions

Guidewire Diameter1.4 Millimeter
Guidewire Length500 Millimeter
Guidewire Diameter1.4 Millimeter
Guidewire Length500 Millimeter
Guidewire Diameter1.4 Millimeter
Guidewire Length500 Millimeter
Guidewire Diameter1.4 Millimeter
Guidewire Length500 Millimeter
Guidewire Diameter1.4 Millimeter
Guidewire Length500 Millimeter
Guidewire Diameter1.4 Millimeter
Guidewire Length500 Millimeter
Guidewire Diameter1.4 Millimeter
Guidewire Length500 Millimeter
Guidewire Diameter1.4 Millimeter
Guidewire Length500 Millimeter
Guidewire Diameter1.4 Millimeter
Guidewire Length500 Millimeter
Guidewire Diameter1.4 Millimeter
Guidewire Length500 Millimeter
Guidewire Diameter1.4 Millimeter
Guidewire Length500 Millimeter
Guidewire Diameter1.4 Millimeter
Guidewire Length500 Millimeter
Guidewire Diameter1.4 Millimeter
Guidewire Length500 Millimeter
Guidewire Diameter1.4 Millimeter
Guidewire Length500 Millimeter
Guidewire Diameter1.4 Millimeter
Guidewire Length500 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100841379106210 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00841379106210]

Moist Heat or Steam Sterilization


[00841379106210]

Moist Heat or Steam Sterilization


[00841379106210]

Moist Heat or Steam Sterilization


[00841379106210]

Moist Heat or Steam Sterilization


[00841379106210]

Moist Heat or Steam Sterilization


[00841379106210]

Moist Heat or Steam Sterilization


[00841379106210]

Moist Heat or Steam Sterilization


[00841379106210]

Moist Heat or Steam Sterilization


[00841379106210]

Moist Heat or Steam Sterilization


[00841379106210]

Moist Heat or Steam Sterilization


[00841379106210]

Moist Heat or Steam Sterilization


[00841379106210]

Moist Heat or Steam Sterilization


[00841379106210]

Moist Heat or Steam Sterilization


[00841379106210]

Moist Heat or Steam Sterilization


[00841379106210]

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.

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00841379139942 - NA2021-06-11 ROD BENDER
00841379139973 - NA2021-06-11 PARALLEL COMPRESSOR
00841379160571 - NA2021-06-11 RATCHETING EGG HANDLE, 1/4 SQ.
00841379160588 - NA2021-06-11 RATCHETING T HANDLE, 1/4 SQ
00841379165262 - NA2021-06-11 MIS TARGETING NEEDLE HOLDER
00841379165477 - NA2021-06-11 MIS GUIDE WIRE GRIPPER
00841379165491 - NA2021-06-11 MIS SCREW DRIVER STYLET, NITINOL

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