Marcon CDSM-8.5

GUDID 00827002217096

Marcon Colon Decompression Set

COOK IRELAND LTD

Colonic decompression tube

• Primary Device ID: 00827002217096
• NIH Device Record Key: e696075e-e9f9-4171-8f5b-db944fda461a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Marcon
• Version Model Number: G21709
• Catalog Number: CDSM-8.5
• Company DUNS: 988559035
• Company Name: COOK IRELAND LTD
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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(812)330-5494
• Email: sharedservices@cookmedical.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store in a dry location, away from temperature extremes

Device Identifiers

Device Issuing Agency	Device ID
GS1	00827002217096 [Primary]

FDA Product Code

• FEG: TUBE, DOUBLE LUMEN FOR INTESTINAL DECOMPRESSION AND/OR INTUBATION

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-03-24
• Device Publish Date: 2016-09-24

On-Brand Devices [Marcon]

• 00827002222182: Marcon Colon Decompression Set
• 00827002219380: Marcon Colon Decompression Set
• 00827002217096: Marcon Colon Decompression Set