“V” Splitter 00-9986-010-13;430002

GUDID 00847538001013

“V” Splitter

SYMMETRY MEDICAL INC.

Orthopaedic chisel

• Primary Device ID: 00847538001013
• NIH Device Record Key: 5bf88086-d8ae-41e4-8a99-28a0b644168d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: “V” Splitter
• Version Model Number: 10-002-000
• Catalog Number: 00-9986-010-13;430002
• Company DUNS: 079881212
• Company Name: SYMMETRY MEDICAL INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00847538001013 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[00847538001013]

Moist Heat or Steam Sterilization

[00847538001013]

Moist Heat or Steam Sterilization

[00847538001013]

Moist Heat or Steam Sterilization

[00847538001013]

Moist Heat or Steam Sterilization

[00847538001013]

Moist Heat or Steam Sterilization

[00847538001013]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-05-20
• Device Publish Date: 2022-05-12

On-Brand Devices [“V” Splitter]

• 00847538006322: “V” Splitter
• 00847538001013: “V” Splitter