Primary Device ID | 04710961935131 |
NIH Device Record Key | 2c1f06f5-c212-4ff0-ad4b-34897dab1122 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Silicone Flat Drain |
Version Model Number | 2014-2101 |
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 | 04710961935131 [Unit of Use] |
GS1 | 14710961935138 [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 | 2022-02-08 |
Device Publish Date | 2022-01-31 |
04710961934950 | 2014-0051 |
04710961935186 | 2014-3102 |
04710961935162 | 2014-3072 |
04710961935148 | 2014-2102 |
04710961935131 | 2014-2101 |
04710961935124 | 2014-2072 |
04710961935117 | 2014-2071 |
04710961935025 | 2014-0132 |
04710961935018 | 2014-0131 |
04710961935001 | 2014-0102 |
04710961934998 | 2014-0101 |
04710961934981 | 2014-0072 |
04710961934974 | 2014-0071 |
04710961934967 | 2014-0052 |