| Primary Device ID | 00889024320536 |
| NIH Device Record Key | c14937ee-1a16-4911-9351-5a13fa0d58ba |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 96-499-60001 |
| Company DUNS | 793120965 |
| Company Name | ZIMMER TRABECULAR METAL TECHNOLOGY 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 | 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 |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmer.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 | |
| 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 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 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024320536 [Primary] |
| FSM | TRAY, SURGICAL, INSTRUMENT |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024320536]
Moist Heat or Steam Sterilization
[00889024320536]
Moist Heat or Steam Sterilization
[00889024320536]
Moist Heat or Steam Sterilization
[00889024320536]
Moist Heat or Steam Sterilization
[00889024320536]
Moist Heat or Steam Sterilization
[00889024320536]
Moist Heat or Steam Sterilization
[00889024320536]
Moist Heat or Steam Sterilization
[00889024320536]
Moist Heat or Steam Sterilization
[00889024320536]
Moist Heat or Steam Sterilization
[00889024320536]
Moist Heat or Steam Sterilization
[00889024320536]
Moist Heat or Steam Sterilization
[00889024320536]
Moist Heat or Steam Sterilization
[00889024320536]
Moist Heat or Steam Sterilization
[00889024320536]
Moist Heat or Steam Sterilization
[00889024320536]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-05-26 |
| 00889024223790 - TM Ardis® | 2020-06-23 |
| 00889024316515 - Mergence™-S | 2020-06-23 |
| 00889024317239 - Mergence™-S | 2020-06-23 |
| 00889024317307 - Mergence™-S | 2020-06-23 |
| 00889024317383 - Mergence™-S | 2020-06-23 |
| 00889024317970 - Mergence™-S | 2020-06-23 |
| 00889024318045 - Mergence™-S | 2020-06-23 |
| 00889024318076 - Mergence™-S | 2020-06-23 |