BAN-11SF, F/G, STERILE BAN-11SF

GUDID 20857878007440

BAN-11SF, F/G, Sterile P/N: 74322-01M

RANFAC CORP.

Bone access cannula

• Primary Device ID: 20857878007440
• NIH Device Record Key: b97ae9dc-b799-4816-81cc-35145fccf0ca
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BAN-11SF, F/G, STERILE
• Version Model Number: 11 Gauge x 13cm
• Catalog Number: BAN-11SF
• Company DUNS: 121622872
• Company Name: RANFAC CORP.
• 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: 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

• Needle Gauge: 11 Gauge

Device Identifiers

Device Issuing Agency	Device ID
GS1	00857878007446 [Primary]
GS1	10857878007443 [Package]; Contains: 00857878007446; Package: Inner Pack [1 Units]; In Commercial Distribution
GS1	20857878007440 [Package]; Contains: 10857878007443; Package: Case [10 Units]; In Commercial Distribution

FDA Product Code

• OCJ: Spinal Channeling Instrument, Vertebroplasty

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-11-25
• Device Publish Date: 2019-11-15

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