Veevo

GUDID 00852189007062

Adult Continuous Intermittent Wall Suction

TENACORE HOLDINGS, INC.

Vacuum suction regulator/regulation set, general-purpose

• Primary Device ID: 00852189007062
• NIH Device Record Key: 8d047c2f-617c-42d9-b63d-135992d35280
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Veevo
• Version Model Number: 1500 Series
• Company DUNS: 138781799
• Company Name: TENACORE HOLDINGS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00852189007062 [Primary]

FDA Product Code

• KDP: Regulator, Vacuum

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: 2016-09-29

On-Brand Devices [Veevo]

• 00861269000299: Pediatric Continuous Only Wall Suction
• 00861269000282: Pediatric Intermittent Only Wall Suction
• 00861269000237: Pediatric Continuous-Intermittent Vacuum Regulator
• 00852189007154: Surgical Continuous Full Wall Suction
• 00852189007130: Adult Continuous Only Wall Suction Regulator
• 00852189007123: Adult Intermittent Only
• 00852189007116: Adult Continuous Full Wall Suction
• 00852189007062: Adult Continuous Intermittent Wall Suction