Endoscopic Biopsy Forceps

GUDID 00643169497757

FORCEPS 3221-002 BIOPSY 2MM L 19.7CM

MEDTRONIC PS MEDICAL, INC.

Flexible endoscopic scissors, reusable

• Primary Device ID: 00643169497757
• NIH Device Record Key: a1c8842a-8449-46d6-b082-707321a9a107
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Endoscopic Biopsy Forceps
• Version Model Number: 3221-002
• Company DUNS: 089055867
• Company Name: MEDTRONIC PS MEDICAL, INC.
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169497757 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K945633

FDA Product Code

• GWG: ENDOSCOPE, NEUROLOGICAL

Sterilization

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

[00643169497757]

Moist Heat or Steam Sterilization

[00643169497757]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-06-13

On-Brand Devices [Endoscopic Biopsy Forceps]

• 00643169498044: FORCEPS 3220-002 BIOPSY 2MM L 28.5CM
• 00643169498037: FORCEPS 3221-001 BIOPSY 3MM L 19.7CM
• 00643169497757: FORCEPS 3221-002 BIOPSY 2MM L 19.7CM
• 00643169497740: FORCEPS 3240-002 GRASPING 2MM L 28.5
• 00643169497733: FORCEPS 3241-002 GRASPING 2MM L 19.7CM