Nuprep Skin Prep Gel 10-25; 10-25S; 10-61; 10-65

GUDID 30891893002247

Single 25g tube of Nuprep Skin Prep Gel (unit of use).

D. O. WEAVER AND COMPANY

Electrode conductive medium

• Primary Device ID: 30891893002247
• NIH Device Record Key: 9a4f8b9c-c33c-4229-a716-37bb960ff360
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nuprep Skin Prep Gel
• Version Model Number: 10-25; 10-25S; 10-61
• Catalog Number: 10-25; 10-25S; 10-61; 10-65
• Company DUNS: 039143201
• Company Name: D. O. WEAVER AND COMPANY
• 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: 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 8005252130
• Email: customerservice@weaverandcompany.com
• Phone: 8005252130
• Email: customerservice@weaverandcompany.com
• Phone: 8005252130
• Email: customerservice@weaverandcompany.com
• Phone: 8005252130
• Email: customerservice@weaverandcompany.com
• Phone: 8005252130
• Email: customerservice@weaverandcompany.com
• Phone: 8005252130
• Email: customerservice@weaverandcompany.com
• Phone: 8005252130
• Email: customerservice@weaverandcompany.com
• Phone: 8005252130
• Email: customerservice@weaverandcompany.com
• Phone: 8005252130
• Email: customerservice@weaverandcompany.com
• Phone: 8005252130
• Email: customerservice@weaverandcompany.com
• Phone: 8005252130
• Email: customerservice@weaverandcompany.com
• Phone: 8005252130
• Email: customerservice@weaverandcompany.com
• Phone: 8005252130
• Email: customerservice@weaverandcompany.com
• Phone: 8005252130
• Email: customerservice@weaverandcompany.com
• Phone: 8005252130
• Email: customerservice@weaverandcompany.com
• Phone: 8005252130
• Email: customerservice@weaverandcompany.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00891893002246 [Primary]
GS1	10891893002243 [Package]; Contains: 00891893002246; Package: Inner Pack [6 Units]; In Commercial Distribution
GS1	20891893002240 [Package]; Contains: 00891893002246; Package: Inner Pack [1 Units]; In Commercial Distribution
GS1	30891893002247 [Package]; Contains: 00891893002246; Package: Inner Pack [1 Units]; In Commercial Distribution
GS1	40891893002244 [Package]; Contains: 00891893002246; Package: Inner Pack [20 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K885306

FDA Product Code

• DRX: Electrode, Electrocardiograph

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2021-10-07
• Device Publish Date: 2016-09-01

On-Brand Devices [Nuprep Skin Prep Gel]

• 30891893002247: Single 25g tube of Nuprep Skin Prep Gel (unit of use).
• 10891893002281: Single-use cup of Nuprep Skin Prep Gel (unit of use)