Comprehensive® Versa-Dial® 110030780

GUDID 00887868231292

Zimmer, Inc.

Reverse shoulder prosthesis head

• Primary Device ID: 00887868231292
• NIH Device Record Key: 34bf9d0b-ebf0-46ea-981d-a1b7ceeb9313
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Comprehensive® Versa-Dial®
• Version Model Number: 110030780
• Catalog Number: 110030780
• Company DUNS: 056038268
• Company Name: Zimmer, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868231292 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K181611

FDA Product Code

• KWT: PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED

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: 2019-03-11
• Device Publish Date: 2019-02-22

On-Brand Devices [Comprehensive® Versa-Dial®]

• 00887868231636: 110030793
• 00887868231629: 110030792
• 00887868231612: 110030791
• 00887868231308: 110030781
• 00887868231292: 110030780
• 00887868231285: 110030779
• 00887868231278: 110030778
• 00887868231261: 110030777
• 00887868231254: 110030776