Bone Marrow Biopsy Needle, RBN-132 RBN-132

GUDID 20857878007587

Bone Marrow Biopsy Needle, RBN-132 P/N 74320-02M

RANFAC CORP.

Bone marrow biopsy needle, single-use

• Primary Device ID: 20857878007587
• NIH Device Record Key: c3cd4139-e4f0-4415-860d-1094c288121a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bone Marrow Biopsy Needle, RBN-132
• Version Model Number: 13 Gauge x 2"
• Catalog Number: RBN-132
• 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: 2 Inch
• Length: 2 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00857878007583 [Primary]
GS1	10857878007580 [Package]; Contains: 00857878007583; Package: Inner Pack [10 Units]; In Commercial Distribution
GS1	20857878007587 [Package]; Contains: 10857878007580; Package: Case [12 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K983187

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: 2018-10-22
• Device Publish Date: 2018-09-21

On-Brand Devices [Bone Marrow Biopsy Needle, RBN-132]

• 20858690006970: Bone Marrow Biopsy Needle, RBN-132 PN 74050-05M
• 20857878007587: Bone Marrow Biopsy Needle, RBN-132 P/N 74320-02M