RAN-811-CT RAN-811-CT

GUDID 20857878007297

RAN-811-CT P/N 74319-01M

RANFAC CORP.

Bone access cannula

• Primary Device ID: 20857878007297
• NIH Device Record Key: 4dd14053-23ec-47a5-88be-8bb6e279b58c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RAN-811-CT
• Version Model Number: 8 Gauge x 11cm
• Catalog Number: RAN-811-CT
• Company DUNS: 121622872
• Company Name: RANFAC CORP.
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 5085884400
• Email: info@ranfac.com

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00857878007293 [Primary]
GS1	10857878007290 [Package]; Contains: 00857878007293; Package: Inner Pack [1 Units]; In Commercial Distribution
GS1	20857878007297 [Package]; Contains: 10857878007290; Package: Case [24 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K131157

FDA Product Code

• KNW: Instrument, Biopsy

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2018-03-01

On-Brand Devices [RAN-811-CT]

• 20857878007389: RAN-811-CT P/N 74276-05M
• 20857878007297: RAN-811-CT P/N 74319-01M
• 20857878007143: RAN-811-CT P/N 74276-01M