Primary Device ID | 10818666020235 |
NIH Device Record Key | 16a83565-5247-41ef-8eb1-4c452d4d2bf0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BodyGuard® Microset w/ 0.2 mic filter and lower y-site with female luer |
Version Model Number | A120-160XYSF |
Company DUNS | 002125419 |
Company Name | CME AMERICA LLC |
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 | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00818666020238 [Primary] |
GS1 | 10818666020235 [Package] Contains: 00818666020238 Package: Case [50 Units] In Commercial Distribution |
FPA | Set, Administration, Intravascular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-06-16 |
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