Ranfac Aspiration Needle, 8GA X 23CM, RAN-823-CT, F/G, Sterile RAN-823-CT

GUDID 20857878007518

RAN-823-CT, F/G, Sterile Part Number: 74315-02M

RANFAC CORP.

Bone access cannula

• Primary Device ID: 20857878007518
• NIH Device Record Key: 379bef42-5fc1-4849-ace2-bbdc2738c97e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ranfac Aspiration Needle, 8GA X 23CM, RAN-823-CT, F/G, Sterile
• Version Model Number: 8GA X 23CM
• Catalog Number: RAN-823-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

• Length: 23 Centimeter
• Length: 23 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00857878007514 [Primary]
GS1	10857878007511 [Package]; Contains: 00857878007514; Package: Inner pack [1 Units]; In Commercial Distribution
GS1	20857878007518 [Package]; Contains: 10857878007511; 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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-01-07
• Device Publish Date: 2018-12-06

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