EIT ALIF Inserter

GUDID 04260397082218

Implant Inserter

EIT Emerging Implant Technologies GmbH

Orthopaedic implant inserter/extractor, reusable

• Primary Device ID: 04260397082218
• NIH Device Record Key: 7a18cd66-7e8f-4998-beea-f0d6f535b1c6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EIT ALIF Inserter
• Version Model Number: AET30100
• Company DUNS: 313088331
• Company Name: EIT Emerging Implant Technologies GmbH
• 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: true
• 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	04260397082218 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K170503

FDA Product Code

• MAX: Intervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

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

[04260397082218]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-04-23
• Device Publish Date: 2018-09-20

On-Brand Devices [EIT ALIF Inserter]

• 04260557774793: Implant inserter knob SH Connection
• 04260557774786: Implant Inserter SH Connection
• 04260557774779: Trial Inserter SH Connection
• 04260397082218: Implant Inserter
• 04260397082201: Trial Inserter