GoodSense

GUDID 10180410000238

Tender Tape, 2 IN x 5 YDS (50 mm x 4.5 m) stretched; 2 IN x 2.2 YDS (50 mm x 2 m)

GEISS, DESTIN & DUNN, INC

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

• Primary Device ID: 10180410000238
• NIH Device Record Key: 39c4a3d8-4076-4dec-9069-7704925c5f67
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GoodSense
• Version Model Number: 180410000231
• Company DUNS: 076059836
• Company Name: GEISS, DESTIN & DUNN, 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00180410000231 [Primary]
GS1	10180410000238 [Package]; Contains: 00180410000231; Package: case [72 Units]; In Commercial Distribution

FDA Product Code

• FQM: Bandage, Elastic

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: 2020-09-07
• Device Publish Date: 2020-08-28

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• 10180410000238: Tender Tape, 2 IN x 5 YDS (50 mm x 4.5 m) stretched; 2 IN x 2.2 YDS (50 mm x 2 m)
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