Avenir Complete™ 574444120
GUDID 00889024510319
Zimmer, Inc.
Surgical implant template, reusable| Primary Device ID | 00889024510319 |
| NIH Device Record Key | 32a6f950-78bf-4054-b3b5-0d37e9f8e2ae |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Avenir Complete™ |
| Version Model Number | 574444120 |
| Catalog Number | 574444120 |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| 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 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com |
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024510319 [Primary] |
FDA Product Code
| HWT | TEMPLATE |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024510319]
Moist Heat or Steam Sterilization
[00889024510319]
Moist Heat or Steam Sterilization
[00889024510319]
Moist Heat or Steam Sterilization
[00889024510319]
Moist Heat or Steam Sterilization
[00889024510319]
Moist Heat or Steam Sterilization
[00889024510319]
Moist Heat or Steam Sterilization
[00889024510319]
Moist Heat or Steam Sterilization
[00889024510319]
Moist Heat or Steam Sterilization
[00889024510319]
Moist Heat or Steam Sterilization
[00889024510319]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-06-24 |
| Device Publish Date | 2019-06-14 |
On-Brand Devices [Avenir Complete™]
Trademark Results [Avenir Complete]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 AVENIR COMPLETE 87563759 not registered Live/Pending |
Zimmer GmbH 2017-08-10 |
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