Spirit® Hydrocolloid Adhesive Sheath 35103

GUDID 10801741070898

Spirit® Hydrocolloid Adhesive Sheath

C. R. Bard, Inc.

Urinary incontinence penis sheath/port, single-use, non-sterile

• Primary Device ID: 10801741070898
• NIH Device Record Key: da51f022-263e-451c-a7a2-3d3e8ebdfe0d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Spirit® Hydrocolloid Adhesive Sheath
• Version Model Number: 35103
• Catalog Number: 35103
• Company DUNS: 016898496
• Company Name: C. R. Bard, 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com

Device Dimensions

• Circumference: 32 Millimeter
• Circumference: 32 Millimeter
• Circumference: 32 Millimeter
• Circumference: 32 Millimeter
• Circumference: 32 Millimeter
• Circumference: 32 Millimeter
• Circumference: 32 Millimeter
• Circumference: 32 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741070891 [Primary]
GS1	10801741070898 [Package]; Contains: 00801741070891; Package: CA [100 Units]; In Commercial Distribution

FDA Product Code

• NNX: DEVICE, INCONTINENCE, UROSHEATH TYPE, NON-STERILE

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-09-27

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