XI.D-RL™ XI.D-RL

GUDID 00885672009632

Disposable Extension Cable

Oscor Inc.

Electrical-only medical device connection cable, single-use

• Primary Device ID: 00885672009632
• NIH Device Record Key: bf923d8e-d55e-4bcc-885d-965b0c35b89a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: XI.D-RL™
• Version Model Number: XI.D-RL
• Catalog Number: XI.D-RL
• Company DUNS: 101835833
• Company Name: Oscor Inc.
• Device Count: 5
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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(727)937-2511
• Email: sales@oscor.com

Device Dimensions

• Length: 250 Centimeter

Operating and Storage Conditions

• Storage Environment Temperature: Between 5 Degrees Celsius and 30 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885672009632 [Unit of Use]
GS1	10885672009639 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K070926

FDA Product Code

• IKD: CABLE, ELECTRODE

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-04-27
• Device Publish Date: 2020-04-17

On-Brand Devices [XI.D-RL™]

• 04260451444013: Disposable Extension Cable
• 00885672009632: Disposable Extension Cable