Primary Device ID | 10885862535115 |
NIH Device Record Key | e792017a-57ea-417c-9ee9-a67f612289d5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vantage |
Version Model Number | 351-90-27 |
Catalog Number | 351-90-27 |
Company DUNS | 157565946 |
Company Name | Exactech, 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 | false |
Serial Number | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10885862535115 [Primary] |
HWT | TEMPLATE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-08-05 |
Device Publish Date | 2022-07-28 |