| Primary Device ID | 00612479227958 |
| NIH Device Record Key | 8aa911c0-fa24-4ec4-8063-9ef78f967dc0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MvKesson |
| Version Model Number | 176-5729 |
| Company DUNS | 023904428 |
| Company Name | MCKESSON MEDICAL-SURGICAL INC. |
| Device Count | 50 |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00612479227941 [Primary] |
| GS1 | 00612479227958 [Package] Contains: 00612479227941 Package: Case [200 Units] In Commercial Distribution |
| GS1 | 00612479240179 [Unit of Use] |
| KOX | Solvent, Adhesive Tape |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-04-01 |
| Device Publish Date | 2019-03-22 |
| 00612479278325 - McKesson | 2025-07-10 FOAM, ADH SIL W/BORDER 5"X5" |
| 10612479274669 - McKesson | 2025-06-26 SCANNER, BLADDER PORTABLE ULTRASOUND |
| 10612479277103 - McKesson | 2025-06-24 Doppler with OLED display, No probe. |
| 10612479277110 - McKesson | 2025-06-24 Doppler no display, No probe. |
| 10612479277127 - McKesson | 2025-06-24 DOPPLER, FETAL HEART, OLED, W/ 2MHZ PROBE |
| 10612479277134 - McKesson | 2025-06-24 DOPPLER, FETAL HEART, OLED, W/ 3MHZ PROBE |
| 10612479277141 - McKesson | 2025-06-24 DOPPLER,VASCULAR, W/ 4MHZ PROBE |
| 10612479277158 - McKesson | 2025-06-24 DOPPLER,VASCULAR, W/ 5MHZ PROBE |