Primary Device ID | 03700512925026 |
NIH Device Record Key | e2c57808-cf61-49f5-b32f-82ef6dcfcb1c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Irrigation Tube |
Version Model Number | OSG00499E10ST35 |
Catalog Number | Z263001 |
Company DUNS | 401020409 |
Company Name | Promepla |
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 | true |
Serial Number | false |
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 | 03700512905028 [Primary] |
GS1 | 03700512915027 [Package] Contains: 03700512905028 Package: Pouch [10 Units] In Commercial Distribution |
GS1 | 03700512925026 [Package] Contains: 03700512915027 Package: Box [10 Units] In Commercial Distribution |
GBX | Catheter, Irrigation |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-04-23 |
Device Publish Date | 2018-04-06 |
03700512925040 | OSG01199E5ST35 |
03700512925033 | OSG01199ST35 |
03700512925026 | OSG00499E10ST35 |
03700512925019 | OSG00499E5ST35 |
03700512925002 | OSG00499ST35 |
03700512915263 | ODG05599E5ST35 |
03700512925071 | OSG03499ST35 |
03700512925064 | OSG03399E5ST35 |