0940035000

GUDID 04546540132277

2.5 inch (63.5mm) Titanium Nitrided Cast Cutter Blade

STRYKER CORPORATION

Cast cutter blade

• Primary Device ID: 04546540132277
• NIH Device Record Key: c80b9f59-e8b5-4452-bdc4-c215af72040a
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 0940035000
• Catalog Number: 0940035000
• Company DUNS: 196548481
• Company Name: STRYKER CORPORATION
• 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: 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)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com

Device Dimensions

• Width: 63.5 Millimeter
• Width: 63.5 Millimeter
• Width: 63.5 Millimeter
• Width: 63.5 Millimeter
• Width: 63.5 Millimeter
• Width: 63.5 Millimeter
• Width: 63.5 Millimeter
• Width: 63.5 Millimeter
• Width: 63.5 Millimeter
• Width: 63.5 Millimeter
• Width: 63.5 Millimeter
• Width: 63.5 Millimeter
• Width: 63.5 Millimeter
• Width: 63.5 Millimeter
• Width: 63.5 Millimeter
• Width: 63.5 Millimeter
• Width: 63.5 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	04546540132277 [Primary]

FDA Product Code

• LGH: INSTRUMENT, CAST REMOVAL, AC-POWERED

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-10-24
• Device Publish Date: 2018-09-23

Devices Manufactured by STRYKER CORPORATION

• 07613327661989 - KNOTILUS+: 2025-06-24 2.9X15.5MM KNOTILUS+ ANCHOR - BIOCOMPOSITE
• 07613327661996 - KNOTILUS+: 2025-06-24 2.4X8.9MM KNOTILUS+ HIP ANCHOR - BIOCOMPOSITE
• 07613327662009 - KNOTILUS+: 2025-06-24 2.4X11.3MM KNOTILUS+ ANCHOR - BIOCOMPOSITE
• 07613327662016 - KNOTILUS+: 2025-06-24 2.9X12.5MM KNOTILUS+ HIP ANCHOR - BIOCOMPOSITE
• 07613327662023 - KNOTILUS+: 2025-06-24 2.9X12.5MM KNOTILUS+ ANCHOR - BIOCOMPOSITE
• 07613327662030 - ALPHAVENT: 2025-06-24 ALPHAVENT KNOTLESS SP, 4.75MM, BIOCOMPOSITE ANCHOR
• 07613327662047 - ALPHAVENT: 2025-06-24 ALPHAVENT KNOTLESS SP, 5.5MM, BIOCOMPOSITE ANCHOR
• 07613327662054 - ALPHAVENT: 2025-06-24 ALPHAVENT KNOTLESS SP, 6.5MM, BIOCOMPOSITE ANCHOR