PECAPLASTY® XMS01050

GUDID 03700879517612

Targeting guide 2.0 wires first

NOVASTEP

General internal orthopaedic fixation system implantation kit

• Primary Device ID: 03700879517612
• NIH Device Record Key: cc304bc4-3d98-41db-b2df-e69cf9003b55
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PECAPLASTY®
• Version Model Number: XMS01050
• Catalog Number: XMS01050
• Company DUNS: 264255288
• Company Name: NOVASTEP
• 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

Customer Support Contacts

• Phone: +33299338650
• Email: contact@novastep-ortho.com
• Phone: +33299338650
• Email: contact@novastep-ortho.com
• Phone: +33299338650
• Email: contact@novastep-ortho.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	03700879517612 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[03700879517612]

Moist Heat or Steam Sterilization

[03700879517612]

Moist Heat or Steam Sterilization

[03700879517612]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-01-23
• Device Publish Date: 2025-01-15

On-Brand Devices [PECAPLASTY®]

• 03700879516455: Sterile traction wire Ø2.5 lg128
• 03700879516448: Traction wire Ø2.5 lg128
• 03700879517612: Targeting guide 2.0 wires first