SSCOR DCell

GUDID B245DM100011

Portable Suction Device

SSCOR, INC.

Emergency airway clearance suction system, electric Emergency airway clearance suction system, electric

• Primary Device ID: B245DM100011
• NIH Device Record Key: 5da2b318-8caf-4cab-8e72-250ece74786b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SSCOR DCell
• Version Model Number: DM10-001
• Company DUNS: 131254971
• Company Name: SSCOR, 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: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B245DM100011 [Primary]

FDA Product Code

• BTA: Pump, Portable, Aspiration (Manual Or Powered)

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: 2018-08-23
• Device Publish Date: 2017-02-13

Devices Manufactured by SSCOR, INC.

• B245150060 - S-SCORT® II: 2021-07-13 Portable Suction Device
• B245150061 - S-SCORT® II: 2018-08-23 Portable Suction Device
• B24521001 - S-SCORT® TEN: 2018-08-23 Portable Suction Device
• B2452100S19 - S-SCORT® TEN: 2018-08-23 Portable Suction Device
• B24521091 - S-SCORT® 9: 2018-08-23 Portable Suction Device
• B245220001 - SSCOR/board: 2018-08-23 Onboard Suction Device
• B24522000BRAUN1 - SSCOR/board: 2018-08-23 Onboard Suction Device
• B24522000GIFA1 - SSCOR/board: 2018-08-23 Onboard Suction Device