Bantex

GUDID 07500463968365

Rubber Band Smarch

Solomed, S.A. de C.V.

Pressure bandage, Hevea-latex, single-use, non-sterile

• Primary Device ID: 07500463968365
• NIH Device Record Key: 58f1e8e2-2fd7-4cb9-bfde-21452e4e8625
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bantex
• Version Model Number: 8cm
• Company DUNS: 588625921
• Company Name: Solomed, S.A. de C.V.
• Device Count: 5
• 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: 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	07500463968365 [Primary]
GS1	17500463968362 [Unit of Use]

FDA Product Code

• MHW: Dressing, Compression

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: 2019-06-14
• Device Publish Date: 2019-06-06

On-Brand Devices [Bantex]

• 07500463968365: Rubber Band Smarch
• 07500463968358: Rubber Band Smarch