REMOVE Adhesive Rem. 237ml CE Mark 59403325

GUDID 30040565122541

Universal adhesive remover

SMITH & NEPHEW MEDICAL LIMITED

Patient medical adhesive remover

• Primary Device ID: 30040565122541
• NIH Device Record Key: ee77ba8a-a83a-40af-bc6e-e050c3e89563
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: REMOVE Adhesive Rem. 237ml CE Mark
• Version Model Number: 59403325
• Catalog Number: 59403325
• 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	00040565122540 [Primary]
GS1	30040565122541 [Package]; Contains: 00040565122540; 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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