OMNI 83-20-50031

GUDID 00812231032909

WOLF LIGHT GUIDE POST ADAPTER

SANTA BARBARA IMAGING SYSTEMS, INC.

Endoscopic light source adaptor

• Primary Device ID: 00812231032909
• NIH Device Record Key: fbd65daf-4e8f-4223-945b-55b023744305
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OMNI
• Version Model Number: 83-20-50031
• Catalog Number: 83-20-50031
• Company DUNS: 065016344
• Company Name: SANTA BARBARA IMAGING SYSTEMS, INC.
• Device Count: 1
• DM Exempt: true
• 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

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	00812231032909 [Primary]

FDA Product Code

• FFY: Adaptor, Bulbs, Miscellaneous, For Endoscope

Sterilization

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

[00812231032909]

Moist Heat or Steam Sterilization

[00812231032909]

Moist Heat or Steam Sterilization

[00812231032909]

Moist Heat or Steam Sterilization

[00812231032909]

Moist Heat or Steam Sterilization

[00812231032909]

Moist Heat or Steam Sterilization

[00812231032909]

Moist Heat or Steam Sterilization

[00812231032909]

Moist Heat or Steam Sterilization

[00812231032909]

Moist Heat or Steam Sterilization

[00812231032909]

Moist Heat or Steam Sterilization

[00812231032909]

Moist Heat or Steam Sterilization

[00812231032909]

Moist Heat or Steam Sterilization

[00812231032909]

Moist Heat or Steam Sterilization

[00812231032909]

Moist Heat or Steam Sterilization

[00812231032909]

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
• 00812231034453: OMNI 4K HDR SYSTEM, TABLET
• 00812231034446: OMNI 4K HDR SYSTEM, CAMERA HEAD, INTEGRATED, 1C
• 00812231034422: OMNI 4K HDR SYSTEM, CAMERA CONTROL UNIT WITH IMAGE CAPTURE & LIGHT ENGINE
• 00812231033470: OMNI 4K HDR SYSTEM, TABLET, TETHERED