Edoscopic Dissection Probe

GUDID 00643169497672

PROBE 3701-003 DISSECT 45 DEG TIP 19.7

MEDTRONIC PS MEDICAL, INC.

Flexible endoscopic scissors, reusable

• Primary Device ID: 00643169497672
• NIH Device Record Key: 44e39861-a5e0-4142-b40f-84e088a19b18
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Edoscopic Dissection Probe
• Version Model Number: 3701-003
• 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	00643169497672 [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

[00643169497672]

Moist Heat or Steam Sterilization

[00643169497672]

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 [Edoscopic Dissection Probe]

• 00643169497702: PROBE 3700-001 DISSECT 90 DEG TIP 28.5
• 00643169497696: PROBE 3700-003 DISSECT 90 DEG TIP 19.7
• 00643169497689: PROBE 3701-001 DISSECT 45 DEG TIP 28.5
• 00643169497672: PROBE 3701-003 DISSECT 45 DEG TIP 19.7