KIM (Knotless Incontinence Mesh)

GUDID 08437007606683

DESARROLLO E INVESTIGACION MEDICA ARAGONESA SL

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• Primary Device ID: 08437007606683
• NIH Device Record Key: c185bb9e-5077-41ad-a53d-4e3066f5699d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KIM (Knotless Incontinence Mesh)
• Version Model Number: KIM-01
• Company DUNS: 513271056
• Company Name: DESARROLLO E INVESTIGACION MEDICA ARAGONESA SL
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• 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	08437007606683 [Primary]

FDA Product Code

• OTN: Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator

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: 2020-10-27
• Device Publish Date: 2020-10-19

On-Brand Devices [KIM (Knotless Incontinence Mesh)]

• 08437007606683: KIM-01
• 08437007606065: KIM01/OID5