Bawmed

GUDID 06975816240008

SUZHOU BAW MEDTECH LTD

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