ZMS®

GUDID 00889024085008

Zimmer, Inc.

Orthopaedic bone wire

• Primary Device ID: 00889024085008
• NIH Device Record Key: 6c25a1e2-81d6-4d05-bad1-24da4b2714e9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ZMS®
• Version Model Number: 47-2237-33
• Company DUNS: 056038268
• Company Name: Zimmer, 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com

Device Dimensions

• Device Size Text, specify: 0
• Length: 100 Centimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024085008 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

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: 2017-02-09

On-Brand Devices [ZMS®]

• 00889024581814: 47-2237-37
• 00889024581807: 47-2237-33
• 00889024581821: 47-2237-38
• 00889024085015: 47-2237-37
• 00889024085008: 47-2237-33
• 00889024041349: 2246-62
• 00889024041325: 2246-23
• 00889024040052: 2239-01
• 00889024039858: 2237-55
• 00889024039841: 2237-54
• 00889024039834: 2237-53
• 00889024039810: 2237-46
• 00889024039773: 2237-37
• 00889024039766: 2237-33
• 00889024039759: 2237-08
• 00889024039742: 2237-05