OMNI 83-20-5002

GUDID 00812231032886

5MM LIGHT GUIDE, GREY

SANTA BARBARA IMAGING SYSTEMS, INC.

Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable

• Primary Device ID: 00812231032886
• NIH Device Record Key: a7338ad5-dd81-41f1-96ac-85e581c4cb1a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OMNI
• Version Model Number: 83-20-5002
• Catalog Number: 83-20-5002
• Company DUNS: 065016344
• Company Name: SANTA BARBARA IMAGING SYSTEMS, INC.
• 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

Customer Support Contacts

• Phone: 805-770-2110
• Email: Info@sbimagingsystems.com
• Phone: 805-770-2110
• Email: Info@sbimagingsystems.com
• Phone: 805-770-2110
• Email: Info@sbimagingsystems.com
• Phone: 805-770-2110
• Email: Info@sbimagingsystems.com
• Phone: 805-770-2110
• Email: Info@sbimagingsystems.com
• Phone: 805-770-2110
• Email: Info@sbimagingsystems.com
• Phone: 805-770-2110
• Email: Info@sbimagingsystems.com
• Phone: 805-770-2110
• Email: Info@sbimagingsystems.com
• Phone: 805-770-2110
• Email: Info@sbimagingsystems.com
• Phone: 805-770-2110
• Email: Info@sbimagingsystems.com
• Phone: 805-770-2110
• Email: Info@sbimagingsystems.com
• Phone: 805-770-2110
• Email: Info@sbimagingsystems.com
• Phone: 805-770-2110
• Email: Info@sbimagingsystems.com
• Phone: 805-770-2110
• Email: Info@sbimagingsystems.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00812231032886 [Primary]

FDA Product Code

• FST: Light, Surgical, Fiberoptic

Sterilization

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

[00812231032886]

Moist Heat or Steam Sterilization

[00812231032886]

Moist Heat or Steam Sterilization

[00812231032886]

Moist Heat or Steam Sterilization

[00812231032886]

Moist Heat or Steam Sterilization

[00812231032886]

Moist Heat or Steam Sterilization

[00812231032886]

Moist Heat or Steam Sterilization

[00812231032886]

Moist Heat or Steam Sterilization

[00812231032886]

Moist Heat or Steam Sterilization

[00812231032886]

Moist Heat or Steam Sterilization

[00812231032886]

Moist Heat or Steam Sterilization

[00812231032886]

Moist Heat or Steam Sterilization

[00812231032886]

Moist Heat or Steam Sterilization

[00812231032886]

Moist Heat or Steam Sterilization

[00812231032886]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-09-25
• Device Publish Date: 2020-09-17

On-Brand Devices [OMNI]

• 00812231032978: 4K UHD CAMERA HEAD, INTEGRATED, 1CMOS, HOLOGIC
• 00812231032831: TABLET, HOLOGIC
• 00812231032961: 4K UHD CAMERA CONTROL UNIT
• 00812231032923: ACMI LIGHT GUIDE POST ADAPTER
• 00812231032916: STORZ LIGHT GUIDE POST ADAPTER
• 00812231032909: WOLF LIGHT GUIDE POST ADAPTER
• 00812231032893: 5MM LIGHT GUIDE, BLUE
• 00812231032886: 5MM LIGHT GUIDE, GREY
• 00812231032947: CAMERA HEAD TRAY, HOLOGIC
• 00812231033531: 4K UHD CAMERA CONTROL UNIT, HOLOGIC, JPN
• 00812231033524: Tablet, Hologic, JPN