SOLO OPOIA20STR

GUDID 05050474521070

I/A HP 20 GA STRAIGHT SILICONE SLV TIP

JOHNSON & JOHNSON SURGICAL VISION, INC.

Ophthalmic surgical procedure kit, non-medicated, reusable

• Primary Device ID: 05050474521070
• NIH Device Record Key: d7e654b6-5b37-406c-bc37-11afdac4c0ae
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SOLO
• Version Model Number: OPOIA20STR
• Catalog Number: OPOIA20STR
• Company DUNS: 103021940
• Company Name: JOHNSON & JOHNSON SURGICAL VISION, INC.
• 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: false
• 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: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	05050474521070 [Primary]

FDA Product Code

• HMX: Cannula, ophthalmic

Sterilization

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

[05050474521070]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-02-26
• Device Publish Date: 2018-11-16

On-Brand Devices [SOLO]

• 05050474521070: I/A HP 20 GA STRAIGHT SILICONE SLV TIP
• 05050474521063: I/A HANDPIECE KIT 20 GA
• 05050474521056: I/A HP 20 GA CURVED SILICONE SLV TIP
• 05050474521049: I/A HP 20 GA 45 DEG SILICONE SLV TIP