Primary Device ID | 00889024570412 |
NIH Device Record Key | 3040f159-2542-43c1-9326-9ba8a8729be5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vanguard |
Version Model Number | SSI000412 |
Catalog Number | SSI000412 |
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 | false |
Serial Number | true |
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) 343-9500 |
customerservice@zimmerbiomet.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024570412 [Primary] |
KIL | Positioner, Socket |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00889024570412]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-03-11 |
Device Publish Date | 2019-02-18 |