AZE300000

GUDID 00840085201431

MIS MODULAR REDUCER DRIVER

HYHTE HOLDINGS, INC.

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• Primary Device ID: 00840085201431
• NIH Device Record Key: 53f0b29c-266b-4c93-9843-3d42ad7939b0
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: AZE300000
• Catalog Number: AZE300000
• 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: false
• 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

Customer Support Contacts

• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM
• Phone: 7608148047
• Email: PARKER@ASTURAMEDICAL.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840085201431 [Primary]

FDA Product Code

• OLO: Orthopedic Stereotaxic Instrument

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00840085201431]

Moist Heat or Steam Sterilization

[00840085201431]

Moist Heat or Steam Sterilization

[00840085201431]

Moist Heat or Steam Sterilization

[00840085201431]

Moist Heat or Steam Sterilization

[00840085201431]

Moist Heat or Steam Sterilization

[00840085201431]

Moist Heat or Steam Sterilization

[00840085201431]

Moist Heat or Steam Sterilization

[00840085201431]

Moist Heat or Steam Sterilization

[00840085201431]

Moist Heat or Steam Sterilization

[00840085201431]

Moist Heat or Steam Sterilization

[00840085201431]

Moist Heat or Steam Sterilization

[00840085201431]

Moist Heat or Steam Sterilization

[00840085201431]

Moist Heat or Steam Sterilization

[00840085201431]

Moist Heat or Steam Sterilization

[00840085201431]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-06-11
• Device Publish Date: 2021-06-03

Devices Manufactured by HYHTE HOLDINGS, INC.

• 00840085265167 - NA: 2024-04-22 CORTICAL CANCELLOUS CANNULATED SCREW
• 00840085265174 - NA: 2024-04-22 CORTICAL CANCELLOUS CANNULATED SCREW
• 00840085265181 - NA: 2024-04-22 CORTICAL CANCELLOUS CANNULATED SCREW
• 00840085265198 - NA: 2024-04-22 CORTICAL CANCELLOUS CANNULATED SCREW
• 00840085265204 - NA: 2024-04-22 CORTICAL CANCELLOUS CANNULATED SCREW
• 00840085265211 - NA: 2024-04-22 CORTICAL CANCELLOUS CANNULATED SCREW
• 00840085265228 - NA: 2024-04-22 CORTICAL CANCELLOUS CANNULATED SCREW
• 00840085265235 - NA: 2024-04-22 CORTICAL CANCELLOUS CANNULATED SCREW