EAFGABBFZ

GUDID 00840085201851

AXIAL HANDLE, ML, ADV 1/4 SQ, FIXED, ALUMINUM CORE, EXTERNAL, CANNULATED, SIDE LOADING SLAP CAP

HYHTE HOLDINGS, INC.

Orthopaedic surgical distractor, internal

• Primary Device ID: 00840085201851
• NIH Device Record Key: f302dbe8-299a-49dc-a727-0cefeb8d2aae
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: EAFGABBFZ
• Catalog Number: EAFGABBFZ
• 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

Customer Support Contacts

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840085201851 [Primary]

FDA Product Code

• OVD: Intervertebral Fusion Device With Integrated Fixation, Lumbar

Sterilization

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

[00840085201851]

Moist Heat or Steam Sterilization

[00840085201851]

Moist Heat or Steam Sterilization

[00840085201851]

Moist Heat or Steam Sterilization

[00840085201851]

Moist Heat or Steam Sterilization

[00840085201851]

Moist Heat or Steam Sterilization

[00840085201851]

Moist Heat or Steam Sterilization

[00840085201851]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-08-11
• Device Publish Date: 2021-08-03

Devices Manufactured by HYHTE HOLDINGS, INC.

• 00840085271861 - NA: 2025-03-06 EGPS, LUMBAR PEDICLE AWL
• 00840085271878 - NA: 2025-03-06 EGPS, LUMBAR PEDICLE PROBE, STRAIGHT
• 00840085271885 - NA: 2025-03-06 EGPS, LUMBAR PEDICLE PROBE, CURVED
• 00840085271892 - NA: 2025-03-06 EGPS, THORACIC PEDICLE PROBE, STRAIGHT
• 00840085271908 - NA: 2025-03-06 EGPS, THORACIC PEDICLE PROBE, CURVED
• 00840085271915 - NA: 2025-03-06 EGPS, REAMING PILOT DRILL, 3.5MM
• 00840085271922 - NA: 2025-03-06 EGPS, CORTICAL, TAP, 3.5MM
• 00840085271939 - NA: 2025-03-06 EGPS, CORTICAL, TAP, 4.0MM