UMG

GUDID 06975239210015

Tangshan UMG Medical Instrument Co.,Ltd

General-purpose absorbent tip applicator/swab, single-use

• Primary Device ID: 06975239210015
• NIH Device Record Key: d572b687-64c9-403d-bd22-6f825a5dcd5c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: UMG
• Version Model Number: U9001
• Company DUNS: 542956376
• Company Name: Tangshan UMG Medical Instrument Co.,Ltd
• 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: true
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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	06975239210015 [Primary]

FDA Product Code

• KXF: Applicator, Absorbent Tipped, Non-Sterile

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: 2023-04-11
• Device Publish Date: 2023-04-03

On-Brand Devices [UMG]

• 06975239210015: U9001
• 06975239210022: U9045