FGS-0268-J

GUDID 07290101361046

DataRecorder 2 Set

Given Imaging, Inc.

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• Primary Device ID: 07290101361046
• NIH Device Record Key: 3516175c-0d7b-4d40-a14a-a52243e6f1e9
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: FGS-0268-J
• Catalog Number: FGS-0268-J
• Company DUNS: 090073722
• Company Name: Given Imaging, 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: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;Fragile
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;Fragile
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;Fragile
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;Fragile
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;Fragile
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;Fragile
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;Fragile
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;Fragile
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;Fragile
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;Fragile
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;Fragile
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;Fragile
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;Fragile
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;Fragile

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290101361046 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K101250

FDA Product Code

• NEZ: SYSTEM, IMAGING, GASTROINTESTINAL, WIRELESS, CAPSULE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-24

Devices Manufactured by Given Imaging, Inc.

• 07290110361068 - GIFD: 2020-01-17 PillCam sensor belt, DR3 C2 SBC
• 04260167480954 - ManoScan: 2019-11-08 AR 3D Probe
• 04260167480961 - ManoScan: 2019-11-08 ESO Catheter, SD Regular
• 04260167482422 - ManoScan: 2019-11-08 ESO 3D Catheter
• 04260167482439 - ManoScan: 2019-11-08 ESO With Extended Tip
• 04260167482446 - ManoScan: 2019-11-08 ESO Z Catheter
• 04260167482453 - ManoScan: 2019-11-08 ESO Catheter, SD Small
• 04260167482460 - ManoScan: 2019-11-08 AR Catheter, Small