Primary Device ID | 30815112020904 |
NIH Device Record Key | 662eddb2-38c3-48ba-a2b1-19d14e68c646 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SaftiCuff DK |
Version Model Number | 900910 |
Catalog Number | 900910 |
Company DUNS | 849234661 |
Company Name | BRACCO DIAGNOSTICS 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 | 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 | 609-514-2200 |
xx@xx.xx |
Catheter Gauge | 48 French |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10815112020900 [Primary] |
GS1 | 30815112020904 [Package] Contains: 10815112020900 Package: Box [75 Units] In Commercial Distribution |
FGD | Catheter, Retention, Barium Enema With Bag |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2020-06-30 |
Device Publish Date | 2016-09-19 |
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30815112021376 - Waste Bottle | 2023-10-24 Waste Bottle for use with CardioGen-82 Infusion System |
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