Primary Device ID | B101A120003XS2YV0 |
NIH Device Record Key | cf3d843c-b198-4fdb-8bec-4d023e78dcb2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BodyGuard® Set with Needleless Y Sites |
Version Model Number | A120-003XS2YV |
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 | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B101A120003XS2YV0 [Primary] |
HIBCC | B101A120003XS2YV1 [Package] Package: Case [12 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 | 2016-08-12 |
10818666020150 | 115 in. (290 cm) For Use with the BodyGuard® Infusion Pump |
B101A120003XS2YV0 | 115 in. (290 cm) For Use with the BodyGuard® Infusion Pump |