RAN-8-301 RAN-8-301

GUDID 00857878007750

RAN-8-301, F/G, STERILE P/N 74150-01M

RANFAC CORP.

Bone access cannula

• Primary Device ID: 00857878007750
• NIH Device Record Key: 87eb6485-f059-4647-b952-0865fcd1fcfd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RAN-8-301
• Version Model Number: 8GA X 11CM
• Catalog Number: RAN-8-301
• 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

• Length: 11 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00857878007750 [Primary]
GS1	10857878007757 [Package]; Package: Inner pack [1 Units]; In Commercial Distribution
GS1	20857878007754 [Package]; Contains: 10857878007757; Package: Case [36 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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-04-26
• Device Publish Date: 2019-04-18

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