LUXOR 48250120

GUDID 07613327266276

BLADE

Stryker Corporation

Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable

• Primary Device ID: 07613327266276
• NIH Device Record Key: e979f75f-eef4-41a4-9914-22cf0110dc23
• Commercial Distribution Discontinuation: 2024-07-04
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LUXOR
• Version Model Number: 48250120
• Catalog Number: 48250120
• Company DUNS: 149183167
• 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: 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 Dimensions

• Length: 120 Millimeter
• Length: 120 Millimeter
• Length: 120 Millimeter
• Length: 120 Millimeter
• Length: 120 Millimeter
• Length: 120 Millimeter
• Length: 120 Millimeter
• Length: 120 Millimeter
• Length: 120 Millimeter
• Length: 120 Millimeter
• Length: 120 Millimeter
• Length: 120 Millimeter
• Length: 120 Millimeter
• Length: 120 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327266276 [Primary]

FDA Product Code

• HAO: INSTRUMENT, SURGICAL, NON-POWERED

Sterilization

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

[07613327266276]

Moist Heat or Steam Sterilization

[07613327266276]

Moist Heat or Steam Sterilization

[07613327266276]

Moist Heat or Steam Sterilization

[07613327266276]

Moist Heat or Steam Sterilization

[07613327266276]

Moist Heat or Steam Sterilization

[07613327266276]

Moist Heat or Steam Sterilization

[07613327266276]

Moist Heat or Steam Sterilization

[07613327266276]

Moist Heat or Steam Sterilization

[07613327266276]

Moist Heat or Steam Sterilization

[07613327266276]

Moist Heat or Steam Sterilization

[07613327266276]

Moist Heat or Steam Sterilization

[07613327266276]

Moist Heat or Steam Sterilization

[07613327266276]

Moist Heat or Steam Sterilization

[07613327266276]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2024-06-26
• Device Publish Date: 2019-11-25

On-Brand Devices [LUXOR]

• 07613327266054: CANNULATED BLUNT DISSECTOR
• 07613327266191: ROD CALIPERS
• 07613327266177: ARM POST
• 07613327266146: SNAKE ARM
• 07613327266061: RETRACTOR BASE
• 07613327121797: FIXATION TRAY TOP INSERT
• 07613327121780: FIXATION TRAY MIDDLE INSERT
• 07613327121773: FIXATION TRAY BOTTOM INSERT
• 07613327121766: RETRACTOR TRAY INSERT
• 07613327119329: LUXOR FIXATION TRAY
• 07613327119312: RETRACTOR TRAY
• 07613327266252: COMPRESSOR
• 07613327266238: DILATOR 5
• 07613327266184: INITIAL DILATOR
• 07613327266030: DILATOR 4
• 07613327266023: DILATOR 3
• 07613327266009: DILATOR 2
• 07613327266214: BAYONETED AWL
• 07613327266382: TAPERED BALL PROBE
• 07613327266245: SCREW HEAD ADJUSTER
• 07613327266207: ROD INTRODUCER
• 07613327266160: BAYONETED BONE PROBE
• 07613327266047: GUIDE PIN
• 07613327266276: BLADE
• 07613327266139: BLADE
• 07613327266115: BLADE
• 07613327266108: BLADE
• 07613327266122: BLADE
• 07613327266092: BLADE
• 07613327266085: BLADE
• 07613327266078: BLADE