VEGA MG987R

GUDID 04046964759864

FEMUR ALIGNMENT PLATE F4-F8

AESCULAP, INC.

Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

• Primary Device ID: 04046964759864
• NIH Device Record Key: bfa6e30b-83f4-4648-8032-f9868d52904c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VEGA
• Version Model Number: MG987R
• Catalog Number: MG987R
• Company DUNS: 082594540
• Company Name: AESCULAP, 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: 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(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04046964759864 [Primary]

FDA Product Code

• LXH: Orthopedic manual surgical instrument

Sterilization

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

[04046964759864]

Moist Heat or Steam Sterilization

[04046964759864]

Moist Heat or Steam Sterilization

[04046964759864]

Moist Heat or Steam Sterilization

[04046964759864]

Moist Heat or Steam Sterilization

[04046964759864]

Moist Heat or Steam Sterilization

[04046964759864]

Moist Heat or Steam Sterilization

[04046964759864]

Moist Heat or Steam Sterilization

[04046964759864]

Moist Heat or Steam Sterilization

[04046964759864]

Moist Heat or Steam Sterilization

[04046964759864]

Moist Heat or Steam Sterilization

[04046964759864]

Moist Heat or Steam Sterilization

[04046964759864]

Moist Heat or Steam Sterilization

[04046964759864]

Moist Heat or Steam Sterilization

[04046964759864]

Moist Heat or Steam Sterilization

[04046964759864]

Moist Heat or Steam Sterilization

[04046964759864]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-10-12
• Device Publish Date: 2022-10-04

On-Brand Devices [VEGA]

• 04046964785146: BOX CHISEL
• 04046964785122: FEMORAL TRIAL PLATE ATTACHMENT ASSEMBLY
• 04046964785115: F7 AND F8 FEMORAL TRIAL PLATE ASSEMBLY
• 04046964785108: F7 AND F8 HEX SLIDE BUSHING ASSEMBLY
• 04046964785092: F4 THRU F6 FEMORAL TRIAL PLATE ASSEMBLY
• 04046964785085: F4 THRU F6 HEX SLIDE BUSHING ASSEMBLY
• 04046964785078: F1 THRU F3 FEMORAL TRIAL PLATE ASSEMBLY
• 04046964785061: F1 THRU F3 HEX SLIDE BUSHING ASSEMBLY
• 04046964760419: F1 4-IN-1 FEMUR CUTTING GUIDE
• 04046964759970: POSTERIOR FEMUR PLATE, 3 DEG RIGHT
• 04046964759956: POSTERIOR FEMUR PLATE, 3 DEG LEFT
• 04046964759925: POSTERIOR FEMUR PLATE, NEUTRAL
• 04046964759895: FEMUR ALIGNMENT PLATE F1-F5
• 04046964757259: ANTERIOR FEMUR STYLUS
• 04046964757235: FEMUR ORIENTATION SLEEVE 5 DEG
• 04046964757228: ANTERIOR FEMUR CUT GUIDE LEFT
• 04046964757211: ANTERIOR FEMUR CUT GUIDE, RIGHT
• 04046964757204: DISTAL FEMUR CUT GUIDE
• 04046964757198: F8 POSTERIOR FEMUR CUT GUIDE
• 04046964757181: F6 POSTERIOR FEMUR CUT GUIDE
• 04046964757174: F5 POSTERIOR FEMUR CUT GUIDE
• 04046964757167: F4 POSTERIOR FEMUR CUT GUIDE
• 04046964757150: F3 POSTERIOR FEMUR CUT GUIDE
• 04046964757143: F2 POSTERIOR FEMUR CUT GUIDE
• 04046964757136: F1 POSTERIOR FEMUR CUT GUIDE
• 04046964757129: F8 4-IN-1 FEMUR CUTTING GUIDE
• 04046964757112: F7 4-IN-1 FEMUR CUTTING GUIDE
• 04046964757105: F6 4-IN-1 FEMUR CUTTING GUIDE
• 04046964757099: F5 4-IN-1 FEMUR CUTTING GUIDE
• 04046964757082: F4 4-IN-1 FEMUR CUTTING GUIDE
• 04046964757075: F3 4-IN-1 FEMUR CUTTING GUIDE
• 04046964757068: F2 4-IN-1 FEMUR CUTTING GUIDE
• 04046964757051: F7 POSTERIOR FEMUR CUT GUIDE
• 04046964759864: FEMUR ALIGNMENT PLATE F4-F8