JULIET ® INSTRUMENTATION JLL-IN 00 03-N

GUDID 07640178982420

BAYONETED BLADE HOLDER

SpineArt SA

Surgical retraction system, reusable

• Primary Device ID: 07640178982420
• NIH Device Record Key: 153efd64-5d74-4818-a05d-15127affb6d0
• Commercial Distribution Discontinuation: 2019-01-14
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: JULIET ® INSTRUMENTATION
• Version Model Number: JLL-IN 00 03-N
• Catalog Number: JLL-IN 00 03-N
• Company DUNS: 483016148
• Company Name: SpineArt SA
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640178982420 [Primary]

FDA Product Code

• GDI: Dissector, Surgical, General & Plastic Surgery

Sterilization

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

[07640178982420]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-02-14
• Device Publish Date: 2019-01-14

On-Brand Devices [JULIET ® INSTRUMENTATION]

• 07640178982420: BAYONETED BLADE HOLDER
• 07640178982413: BAYONETED PENFIELD #4, TOE OUT
• 07640178982406: BAYONETED PENFIELD #4, TOE IN
• 07640178981638: COMPACTION BASE
• 07640178981621: TRIAL IMPLANT Ti TL
• 07640178981614: TRIAL IMPLANT Ti TL
• 07640178981607: TRIAL IMPLANT Ti TL
• 07640178981591: TRIAL IMPLANT Ti TL
• 07640178981584: TRIAL IMPLANT Ti TL
• 07640178981577: TRIAL IMPLANT Ti TL
• 07640178981560: TRIAL IMPLANT Ti TL
• 07640178981553: TRIAL IMPLANT Ti TL
• 07640178981546: TRIAL IMPLANT Ti TL
• 07640178981539: TRIAL IMPLANT Ti PO/OL SMALL WIDTH
• 07640178981522: TRIAL IMPLANT Ti PO/OL SMALL WIDTH
• 07640178981515: TRIAL IMPLANT Ti PO/OL SMALL WIDTH
• 07640178981508: TRIAL IMPLANT Ti PO/OL SMALL WIDTH
• 07640178981492: TRIAL IMPLANT Ti PO/OL SMALL WIDTH
• 07640178981485: TRIAL IMPLANT Ti PO/OL SMALL WIDTH
• 07640178981478: TRIAL IMPLANT Ti PO/OL SMALL WIDTH
• 07640178981461: TRIAL IMPLANT Ti PO/OL SMALL WIDTH
• 07640178981454: TRIAL IMPLANT Ti PO/OL SMALL WIDTH
• 07640178981447: TRIAL IMPLANT Ti PO/OL SMALL WIDTH
• 07640178981430: TRIAL IMPLANT Ti PO/OL
• 07640178981423: TRIAL IMPLANT Ti PO/OL
• 07640178981416: TRIAL IMPLANT Ti PO/OL
• 07640178981409: TRIAL IMPLANT Ti PO/OL
• 07640178981393: TRIAL IMPLANT Ti PO/OL
• 07640178981386: TRIAL IMPLANT Ti PO/OL
• 07640178981379: TRIAL IMPLANT Ti PO/OL
• 07640178981362: TRIAL IMPLANT Ti PO/OL
• 07640178981355: TRIAL IMPLANT Ti PO/OL
• 07640178981348: TRIAL IMPLANT Ti PO/OL
• 07640178972728: SLAP HAMMER ATTACHMENT
• 07640178972490: DISC SHAVER H14
• 07640178972483: DISC SHAVER H12
• 07640178972476: DISC SHAVER H10
• 07640178972469: DISC SHAVER H08
• 07640178971608: HANDLE DISC PREP
• 07640178971592: TEARDROP CURETTE LATERAL ANGLED
• 07640178971585: TEARDROP CURETTE STRAIGHT
• 07640178971578: RASP DOUBLE SIDED STRAIGHT
• 07640178971561: CUP CURETTE # 1 ANGLED UP
• 07640178971554: CUP CURETTE # 1 RIGHT 45°
• 07640178971547: CUP CURETTE # 1 LEFT 45°
• 07640178971530: CUP CURETTE # 1 STRAIGHT
• 07640151113100: PADDLE DISTRACTOR 16
• 07640151113094: PADDLE DISTRACTOR 14
• 07640151113087: PADDLE DISTRACTOR 12
• 07640151113070: PADDLE DISTRACTOR 10