General Instrument 2014-0008

GUDID 00190837090227

DRILL, 4.5mm

Life Spine, Inc.

Surgical retraction system, reusable

• Primary Device ID: 00190837090227
• NIH Device Record Key: 6f33e137-78da-4f64-8c22-ea1621bf628f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: General Instrument
• Version Model Number: 2014-0008
• Catalog Number: 2014-0008
• 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	00190837090227 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[00190837090227]

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 Instrument]

• 00190837089467: 112-495
• 00190837089450: 112-490
• 00190837089337: 113-954
• 00190837089320: 113-131
• 00190837085148: 113-118
• 00190837079536: 113-117
• 00190837079529: 113-116
• 00190837079512: 113-103
• 00190837090227: DRILL, 4.5mm
• 00190837090210: DRILL, 4.0mm