General Manual Instrument 113-084

GUDID 00190837079239

T30 Driver

Life Spine, Inc.

Surgical retraction system, reusable

• Primary Device ID: 00190837079239
• NIH Device Record Key: 5c454279-e2cf-441f-8443-e1ac06df6625
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: General Manual Instrument
• Version Model Number: 113-084
• Catalog Number: 113-084
• Company DUNS: 183641617
• Company Name: Life Spine, Inc.
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00190837079239 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[00190837079239]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-11-27
• Device Publish Date: 2019-11-19

On-Brand Devices [General Manual Instrument]

• 00190837102586: Access Chisel
• 00190837102579: Access Chisel
• 00190837079239: T30 Driver