Primary Device ID | 10816317022409 |
NIH Device Record Key | ad1c86bd-2afc-411d-acf3-2cd89ecae89e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vital Signs |
Version Model Number | RM-IN900012 |
Company DUNS | 100439103 |
Company Name | RENU MEDICAL, INC |
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 | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
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 | 00816317022402 [Primary] |
GS1 | 10816317022409 [Package] Contains: 00816317022402 Package: Case [12 Units] In Commercial Distribution |
KZD | Infusor, Pressure, For I.V. Bags |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-07-05 |
Device Publish Date | 2023-06-27 |
10816317022409 | Vital Signs Pressure Infusor Bag 1000cc |
10816317022379 | Vital Signs Pressure Infusor Bag 500cc |