Bawmed

GUDID 06975816240008

SUZHOU BAW MEDTECH LTD

Medical air terminal unit Medical air terminal unit Medical air terminal unit Medical air terminal unit Medical air terminal unit Medical air terminal unit Medical air terminal unit Medical air terminal unit Medical air terminal unit Medical air terminal unit Medical air terminal unit Medical air terminal unit Medical air terminal unit Medical air terminal unit Medical air terminal unit Medical air terminal unit

• Primary Device ID: 06975816240008
• NIH Device Record Key: 7e0b482a-7a79-428c-a0d2-3be2cbc29b2e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bawmed
• Version Model Number: BM-DS wall
• Company DUNS: 542992754
• Company Name: SUZHOU BAW MEDTECH LTD
• Device Count: 14
• 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: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06975816240008 [Unit of Use]
GS1	16975816240005 [Primary]

FDA Product Code

• BXY: Flowmeter, Calibration, Gas

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-11-11
• Device Publish Date: 2022-11-03

On-Brand Devices [Bawmed]

• 06975816240008: BM-DS wall
• 06975816240053: BM-SJ-2L-02