PERLA TL NAV NAV-IN 51 31-N

GUDID 07640332471623

DRILL Ø3.1

SpineArt SA

Bone tap, reusable

• Primary Device ID: 07640332471623
• NIH Device Record Key: cc45c24d-b598-421f-86e8-170acd9a7985
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PERLA TL NAV
• Version Model Number: NAV-IN 51 31-N
• Catalog Number: NAV-IN 51 31-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 Dimensions

• Outer Diameter: 6 Millimeter
• Outer Diameter: 6 Millimeter
• Outer Diameter: 6 Millimeter
• Outer Diameter: 6 Millimeter
• Outer Diameter: 6 Millimeter
• Outer Diameter: 6 Millimeter
• Outer Diameter: 6 Millimeter
• Outer Diameter: 6 Millimeter
• Outer Diameter: 6 Millimeter
• Outer Diameter: 6 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640332471623 [Primary]

FDA Product Code

• OLO: Orthopedic Stereotaxic Instrument

Sterilization

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

[07640332471623]

Moist Heat or Steam Sterilization

[07640332471623]

Moist Heat or Steam Sterilization

[07640332471623]

Moist Heat or Steam Sterilization

[07640332471623]

Moist Heat or Steam Sterilization

[07640332471623]

Moist Heat or Steam Sterilization

[07640332471623]

Moist Heat or Steam Sterilization

[07640332471623]

Moist Heat or Steam Sterilization

[07640332471623]

Moist Heat or Steam Sterilization

[07640332471623]

Moist Heat or Steam Sterilization

[07640332471623]

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

Devices Manufactured by SpineArt SA

• 07640185349650 - PERLA ® TL: 2025-11-28 CANNULATED CORTICAL SCREWDRIVER SHAFT
• 07640270064178 - CURE ACP: 2025-11-28 ANTERIOR CERVICAL PLATE, 1 LEVEL L18
• 07640270064192 - CURE ACP: 2025-11-28 ANTERIOR CERVICAL PLATE, 1 LEVEL L20
• 07640270064215 - CURE ACP: 2025-11-28 ANTERIOR CERVICAL PLATE, 1 LEVEL L22
• 07640270064239 - CURE ACP: 2025-11-28 ANTERIOR CERVICAL PLATE, 1 LEVEL L24
• 07640270064291 - CURE ACP: 2025-11-28 ANTERIOR CERVICAL PLATE, 1 LEVEL L30
• 07640270064345 - CURE ACP: 2025-11-28 ANTERIOR CERVICAL PLATE, 1 LEVEL L20
• 07640270064475 - CURE ACP: 2025-11-28 ANTERIOR CERVICAL PLATE, 2 LEVELS L30