JUVEDERM ULTRA PLUS 94143-2

GUDID 30888628000043

Juvederm Ultra Plus 27G 1x0,8mL

Allergan, Inc.

Dermal tissue reconstructive material, microbe-derived

• Primary Device ID: 30888628000043
• NIH Device Record Key: 3eb67aeb-58dc-40cb-a032-7dbddad130f1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: JUVEDERM ULTRA PLUS
• Version Model Number: 94143-2
• Catalog Number: 94143-2
• Company DUNS: 144796497
• Company Name: Allergan, Inc.
• 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: 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: 8006244261
• Email: ProductSupport@allergan.com
• Phone: 8006244261
• Email: ProductSupport@allergan.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0

Operating and Storage Conditions

• Storage Environment Temperature: Between 2 Degrees Celsius and 25 Degrees Celsius
• Storage Environment Temperature: Between 2 Degrees Celsius and 25 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	10888628000049 [Primary]
GS1	30888628000043 [Package]; Contains: 10888628000049; Package: Box [2 Units]; In Commercial Distribution

FDA Product Code

• LMH: Implant, Dermal, For Aesthetic Use

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2014-09-17

On-Brand Devices [JUVEDERM ULTRA PLUS]

• 30888628000050: Juvederm Ultra Plus 27G 2x0.4mL
• 30888628000043: Juvederm Ultra Plus 27G 1x0,8mL