Primary Device ID | 04710961935711 |
NIH Device Record Key | fe49d3db-1b1d-40e9-ad80-e6ed29c1c841 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Silicone Round Drain |
Version Model Number | 2015-0320 |
Company DUNS | 656763489 |
Company Name | FORTUNE MEDICAL INSTRUMENT CORP. |
Device Count | 10 |
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 | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04710961935711 [Unit of Use] |
GS1 | 14710961935718 [Primary] |
GCD | Connector, Catheter |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-01-17 |
Device Publish Date | 2022-01-07 |
04711182607395 | 2015-0314 |
04711182607388 | 2015-0312 |
04711182607371 | 2015-0212 |
04710961935711 | 2015-0320 |
04710961935704 | 2015-0318 |
04710961935698 | 2015-0316 |
04710961935681 | 2015-0310 |
04710961935674 | 2015-0308 |
04710961935605 | 2015-0220 |
04710961935599 | 2015-0218 |
04710961935582 | 2015-0216 |
04710961935575 | 2015-0214 |
04710961935568 | 2015-0210 |
04710961935551 | 2015-0208 |