Frame Adapter for Leibinger RM™ 66-FA-RM

GUDID 00873263006177

Frame Adapter for Leibinger RM™ for use with microTargeting™ Drive, 1X

FHC, INC.

Neurosurgical micro targeting drive

• Primary Device ID: 00873263006177
• NIH Device Record Key: 4c425c31-e50b-4655-a569-d16bd51efb00
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Frame Adapter for Leibinger RM™
• Version Model Number: 66-FA-RM-00616
• Catalog Number: 66-FA-RM
• Company DUNS: 108179458
• Company Name: FHC, INC.
• 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: false
• 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

Customer Support Contacts

• Phone: +1(800)326-2905
• Email: fhcinc@fh-co.com

Operating and Storage Conditions

• Storage Environment Temperature: Between -34 Degrees Celsius and 57 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00873263006160 [Primary]
GS1	00873263006177 [Direct Marking]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K011992

FDA Product Code

• HAW: Neurological stereotaxic Instrument

Sterilization

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

[00873263006177]

Moist Heat or Steam Sterilization;Hydrogen Peroxide;Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-08-01

On-Brand Devices [Frame Adapter for Leibinger RM™]

• 00873263006177: Frame Adapter for Leibinger RM™ for use with microTargeting™ Drive, 1X
• 00873263006160: Frame Adapter for Leibinger RM™ for use with microTargeting™ Drive, 1X