| Primary Device ID | 10818666020365 |
| NIH Device Record Key | 16c70cb2-0c9a-49e9-beda-38930c0fbf3a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BodyGuard® Microset With Female Luer |
| Version Model Number | A120-160XPSN |
| 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 | 00818666020368 [Primary] |
| GS1 | 10818666020365 [Package] Contains: 00818666020368 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 | 2017-06-21 |
| 10818666020365 | 12 in. (30 cm) Microset with Female Luer - Blue Stripe, For Use with the BodyGuard® Infusion Pu |
| B101A120160XPSN1 | 12 in. (30 cm) Microset with Female Luer - Blue Stripe, For Use with the BodyGuard® Infusion Pu |