PERLA NAV NAV-IN 20 11-N

GUDID 07640332471692

LOCKING SCREWDRIVER

SpineArt SA

Surgical screwdriver, reusable

• Primary Device ID: 07640332471692
• NIH Device Record Key: 31d51854-d6d4-4021-a253-4635d7dc1caa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PERLA NAV
• Version Model Number: NAV-IN 20 11-N
• Catalog Number: NAV-IN 20 11-N
• Company DUNS: 483016148
• Company Name: SpineArt SA
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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	07640332471692 [Primary]

FDA Product Code

• OLO: Orthopedic Stereotaxic Instrument

Sterilization

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

[07640332471692]

Moist Heat or Steam Sterilization

[07640332471692]

Moist Heat or Steam Sterilization

[07640332471692]

Moist Heat or Steam Sterilization

[07640332471692]

Moist Heat or Steam Sterilization

[07640332471692]

Moist Heat or Steam Sterilization

[07640332471692]

Moist Heat or Steam Sterilization

[07640332471692]

Moist Heat or Steam Sterilization

[07640332471692]

Moist Heat or Steam Sterilization

[07640332471692]

Moist Heat or Steam Sterilization

[07640332471692]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-11-28
• Device Publish Date: 2025-11-20

On-Brand Devices [PERLA NAV]

• 07640332471708: LOCKING SCREWDRIVER CANNULATED
• 07640332471692: LOCKING SCREWDRIVER
• 07640332471616: DRILL Ø2.4