ANAX™ OCT SPINAL SYSTEM

GUDID 08800037548269

U&I CORPORATION

Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting

• Primary Device ID: 08800037548269
• NIH Device Record Key: c7f3eb24-db98-4077-8a60-3d93f5e6cc63
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ANAX™ OCT SPINAL SYSTEM
• Version Model Number: OS0030
• Company DUNS: 688811082
• Company Name: U&I CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800037548269 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

[08800037548269]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-07-16
• Device Publish Date: 2021-07-08

On-Brand Devices [ANAX™ OCT SPINAL SYSTEM]

• 08800037502216: OSA4150
• 08800037502209: OSA4148
• 08800037502193: OSA4146
• 08800037502186: OSA4144
• 08800037502179: OSA4142
• 08800037502162: OSA4140
• 08800037502155: OSA4138
• 08800037502148: OSA4136
• 08800037502131: OSA4134
• 08800037502124: OSA4132
• 08800037502117: OSA4130
• 08800037502100: OSA4128
• 08800037502094: OSA4126
• 08800037502087: OSA4124
• 08800037502070: OSA4122
• 08800037502063: OSA4120
• 08800037502056: OSA3650
• 08800037502049: OSA3648
• 08800037502032: OSA3646
• 08800037502025: OSA3644
• 08800037502018: OSA3642
• 08800037502001: OSA3640
• 08800037501998: OSA3638
• 08800037504326: OSS0320
• 08800037504319: OSS0310
• 08800015909570: OSA5130
• 08800015909563: OSA5120
• 08800015909556: OSA5110
• 08800015909549: OSA5030
• 08800015909532: OSA5020
• 08800015909525: OSA5010
• 08800015909518: OSA4550
• 08800015909501: OSA4548
• 08800015909495: OSA4546
• 08800015909488: OSA4544
• 08800015909471: OSA4542
• 08800015909464: OSA4540
• 08800015909457: OSA4538
• 08800015909440: OSA4536
• 08800015909433: OSA4534
• 08800015909426: OSA4532
• 08800015909419: OSA4530
• 08800015909402: OSA4528
• 08800015909396: OSA4526
• 08800015909389: OSA4524
• 08800015909372: OSA4522
• 08800015909365: OSA4520
• 08800015909358: OSA4050
• 08800015909341: OSA4048
• 08800015909334: OSA4046