REMOVE Adhesive Remover 8oz US 403300

GUDID 30040565112436

Universal adhesive remover wipe

SMITH & NEPHEW MEDICAL LIMITED

Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover Patient medical adhesive remover

• Primary Device ID: 30040565112436
• NIH Device Record Key: 7c594818-629a-4c50-a958-05464d9df28d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: REMOVE Adhesive Remover 8oz US
• Version Model Number: 403300
• Catalog Number: 403300
• Company DUNS: 216344051
• Company Name: SMITH & NEPHEW MEDICAL LIMITED
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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	00040565112435 [Primary]
GS1	30040565112436 [Package]; Contains: 00040565112435; Package: Case [12 Units]; In Commercial Distribution

FDA Product Code

• KOX: Solvent, Adhesive Tape

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: 2020-09-14
• Device Publish Date: 2020-09-04

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