Primary Device ID | 00889024316362 |
NIH Device Record Key | 9c84bd85-4395-44a4-83c1-a07f8ee8d8ae |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Mergence™-S |
Version Model Number | 96-101-03071 |
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 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024316362 [Primary] |
HXB | PROBE |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00889024316362]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-02-07 |
Device Publish Date | 2017-09-20 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() MERGENCE 77052371 3606453 Live/Registered |
Zimmer Biomet Spine, Inc. 2006-11-28 |