GUDID 00763000054281

HAMMER 9734592 SLAP

MEDTRONIC POWERED SURGICAL SOLUTIONS

Surgical mallet Surgical mallet Surgical mallet Surgical mallet Surgical mallet Surgical mallet Surgical mallet Surgical mallet Surgical mallet Surgical mallet Surgical mallet Surgical mallet Surgical mallet Surgical mallet

• Primary Device ID: 00763000054281
• NIH Device Record Key: 6b4a2a63-d05b-4b5b-9721-b3c74a3f4029
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 9734592
• Company DUNS: 098308849
• Company Name: MEDTRONIC POWERED SURGICAL SOLUTIONS
• Device Count: 1
• DM Exempt: true
• 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
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• 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	00763000054281 [Primary]

FDA Product Code

• FZY: HAMMER, SURGICAL

Sterilization

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

[00763000054281]

Moist Heat or Steam Sterilization

[00763000054281]

Moist Heat or Steam Sterilization

[00763000054281]

Moist Heat or Steam Sterilization

[00763000054281]

Moist Heat or Steam Sterilization

[00763000054281]

Moist Heat or Steam Sterilization

[00763000054281]

Moist Heat or Steam Sterilization

[00763000054281]

Moist Heat or Steam Sterilization

[00763000054281]

Moist Heat or Steam Sterilization

[00763000054281]

Moist Heat or Steam Sterilization

[00763000054281]

Moist Heat or Steam Sterilization

[00763000054281]

Moist Heat or Steam Sterilization

[00763000054281]

Moist Heat or Steam Sterilization

[00763000054281]

Moist Heat or Steam Sterilization

[00763000054281]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-07-31
• Device Publish Date: 2020-07-23

Devices Manufactured by MEDTRONIC POWERED SURGICAL SOLUTIONS

• 00763000732943 - MR8: 2024-01-26 TOOL MR8-ND13BA30D MR8 13CM ND B D 3MM
• 00763000732967 - MR8: 2024-01-26 TOOL MR8-SD12BA30D MR8 12CM SD B D 3MM
• 00763000732974 - MR8: 2024-01-26 TOOL MR8-SD12BA40D MR8 12CM SD B D 4MM
• 00763000732981 - MR8: 2024-01-26 TOOL MR8-SD12BA30DC MR8 12CM SD B DC3MM
• 00763000732998 - MR8: 2024-01-26 TOOL MR8-SD12BA40DC MR8 12CM SD B DC4MM
• 00763000737276 - MR8: 2024-01-26 TOOL MR8-ND13BA40D MR8 13CM ND B D 4MM
• 00763000651152 - MR8: 2023-12-11 TOOL MR8-15MH30SH MR8 15CM 3MM MATCH SH
• 00763000714635 - MR8: 2023-12-11 TOOL MR8-10MH30SH 10CM MATCH 3MM SHORT