ADDTO 2221

GUDID 00860001236019

Catheter Plug And Tube Tip Protector

Addto

Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage Urethral catheterization support kit, urinary drainage

• Primary Device ID: 00860001236019
• NIH Device Record Key: 98a04550-2651-4ffc-a7fd-a1050e8b92fa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ADDTO
• Version Model Number: 2221
• Catalog Number: 2221
• Company DUNS: 076860139
• Company Name: Addto
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860001236019 [Primary]
GS1	00860001236040 [Package]; Package: Box [100 Units]; In Commercial Distribution
GS1	00860001236057 [Package]; Contains: 00860001236040; Package: Case [8 Units]; In Commercial Distribution

FDA Product Code

• GCE: Adaptor, Catheter

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: 2020-07-23
• Device Publish Date: 2020-07-15

On-Brand Devices [ADDTO]

• 00860001236071: Invalid Cushion
• 00860001236019: Catheter Plug And Tube Tip Protector
• 00860001236026: Catheter Adapter