Primary Device ID | 10885862546241 |
NIH Device Record Key | fe7489df-64cf-42a0-b995-90b6caa02ff9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vantage |
Version Model Number | 350-03-02 |
Catalog Number | 350-03-02 |
Company DUNS | 157565946 |
Company Name | Exactech, 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 | 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 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 | 10885862546241 [Primary] |
HSN | Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-11-21 |
Device Publish Date | 2019-11-13 |