TYTEK TRAUMA BANDAGE TM-204

GUDID 00855204008068

4" Trauma Bandage

TYTEK MEDICAL INC.

First aid gauze/bandage

• Primary Device ID: 00855204008068
• NIH Device Record Key: 0a0552f9-7d83-4f9a-8a7f-8d11b2857999
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TYTEK TRAUMA BANDAGE
• Version Model Number: TM-204
• Catalog Number: TM-204
• Company DUNS: 078589992
• Company Name: TYTEK MEDICAL 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: true
• 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	00855204008068 [Primary]

FDA Product Code

• FQM: Bandage, Elastic

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-10-11
• Device Publish Date: 2019-10-03

On-Brand Devices [TYTEK TRAUMA BANDAGE]

• 00855204008082: Abdominal Trauma Bandage
• 00855204008075: 6" Trauma Bandage
• 00855204008068: 4" Trauma Bandage