Primary Device ID | 03700512921165 |
NIH Device Record Key | 20eab9ec-9f36-4c1f-9d00-4af5d11571ca |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Urology - 1 WAY TURP / POST OPERATIVE Irrigation/Aspiration set |
Version Model Number | SOUR9212ST12 |
Catalog Number | SOUR9212ST12 |
Company DUNS | 401020409 |
Company Name | Promepla |
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 | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +37797984232 |
customer@rocamed.eu |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03700512901167 [Primary] |
GS1 | 03700512911166 [Package] Contains: 03700512901167 Package: Box label 1 [15 Units] In Commercial Distribution |
GS1 | 03700512921165 [Package] Contains: 03700512911166 Package: Box label 2 [2 Units] In Commercial Distribution |
FHF | System, Evacuator, Fluid |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2019-11-11 |
Device Publish Date | 2016-10-11 |