Endoscope Storz Light Cable Adapter

GUDID 00643169498266

ADAPTER 5196-903 STORZ USE W 5196-001

MEDTRONIC PS MEDICAL, INC.

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• Primary Device ID: 00643169498266
• NIH Device Record Key: 68d77e99-ff7b-4473-acc7-bb7d886b3d34
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Endoscope Storz Light Cable Adapter
• Version Model Number: 5196-903
• Company DUNS: 089055867
• Company Name: MEDTRONIC PS MEDICAL, 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: 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(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169498266 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K010341

FDA Product Code

• GWG: ENDOSCOPE, NEUROLOGICAL

Sterilization

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

[00643169498266]

Ethylene Oxide

[00643169498266]

Ethylene Oxide

[00643169498266]

Ethylene Oxide

[00643169498266]

Ethylene Oxide

[00643169498266]

Ethylene Oxide

[00643169498266]

Ethylene Oxide

[00643169498266]

Ethylene Oxide

[00643169498266]

Ethylene Oxide

[00643169498266]

Ethylene Oxide

[00643169498266]

Ethylene Oxide

[00643169498266]

Ethylene Oxide

[00643169498266]

Ethylene Oxide

[00643169498266]

Ethylene Oxide

[00643169498266]

Ethylene Oxide

[00643169498266]

Ethylene Oxide

[00643169498266]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-06-13

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