Trimed

GUDID 00822383295558

Trimed, Sportneb

Drive Devilbiss Healthcare

Nebulizing system, non-heated

• Primary Device ID: 00822383295558
• NIH Device Record Key: a1ff2c2e-86cf-43b2-8d67-dc79807fb0cf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Trimed
• Version Model Number: 3050-2-Trimedb
• Company DUNS: 867673159
• Company Name: Drive Devilbiss Healthcare
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00822383295558 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K003344

FDA Product Code

• CAF: NEBULIZER (DIRECT PATIENT INTERFACE)

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: 2018-07-06
• Device Publish Date: 2016-09-16

Devices Manufactured by Drive Devilbiss Healthcare

• 00822383030333 - Drive: 2025-09-11
• 00822383000190 - Drive: 2025-09-10 35" BRNWOOD BEDEND W/SC05,OSLO FM,EA
• 00822383000206 - Drive: 2025-09-10 35" MILL CRK BEDEND W/SC05, OSLO OAK,EA
• 00822383000213 - Drive: 2025-09-10 35" MILL CRK BEDEND W/SC05,OSLO CHERRY,EA
• 00822383000220 - Drive: 2025-09-10 35" MILL CRK BEDEND W/SC05,OSLO FM,EA
• 00822383000237 - Drive: 2025-09-10 42" BRNWOOD BEDEND W/SC05,OSLO OAK,EA
• 00822383000244 - Drive: 2025-09-10 42" BRNWOOD BEDEND W/SC05,OSLO CHERRY,EA
• 00822383000251 - Drive: 2025-09-10 42" BRNWOOD BEDEND W/SC05,OSLO FM,EA