PERLA® TL MIS MPF-IN 07 00-N

GUDID 07640305165481

PROTECTIVE CANNULA

SpineArt SA

Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable

• Primary Device ID: 07640305165481
• NIH Device Record Key: 75e844d7-b56c-477d-ba23-bf23a7ab3f90
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PERLA® TL MIS
• Version Model Number: MPF-IN 07 00-N
• Catalog Number: MPF-IN 07 00-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	07640305165481 [Primary]

FDA Product Code

• KWP: Appliance, Fixation, Spinal Interlaminal

Sterilization

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

[07640305165481]

Moist Heat or Steam Sterilization

[07640305165481]

Moist Heat or Steam Sterilization

[07640305165481]

Moist Heat or Steam Sterilization

[07640305165481]

Moist Heat or Steam Sterilization

[07640305165481]

Moist Heat or Steam Sterilization

[07640305165481]

Moist Heat or Steam Sterilization

[07640305165481]

Moist Heat or Steam Sterilization

[07640305165481]

Moist Heat or Steam Sterilization

[07640305165481]

Moist Heat or Steam Sterilization

[07640305165481]

Moist Heat or Steam Sterilization

[07640305165481]

Moist Heat or Steam Sterilization

[07640305165481]

Moist Heat or Steam Sterilization

[07640305165481]

Moist Heat or Steam Sterilization

[07640305165481]

Moist Heat or Steam Sterilization

[07640305165481]

Moist Heat or Steam Sterilization

[07640305165481]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-07-05
• Device Publish Date: 2023-06-27

On-Brand Devices [PERLA® TL MIS]

• 07640305165511: ALIGNMENT GUIDE
• 07640305165504: ALIGNMENT GUIDE MIS
• 07640305165498: PROTECTIVE CANNULA
• 07640305165481: PROTECTIVE CANNULA