EIT ALIF Distractor Forceps

GUDID 04260397082133

Distractor Forceps

EIT Emerging Implant Technologies GmbH

Bone distraction forceps

• Primary Device ID: 04260397082133
• NIH Device Record Key: 2d8fab9c-3944-4d7b-a788-e84999e63b05
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EIT ALIF Distractor Forceps
• Version Model Number: AET10100
• 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	04260397082133 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K170503

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[04260397082133]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2018-01-05

On-Brand Devices [EIT ALIF Distractor Forceps]

• 04260557774694: Offset Distractor Forceps
• 04260397082133: Distractor Forceps