Primary Device ID | 20884527006448 |
NIH Device Record Key | 62027450-8e47-4bd5-b212-167f9dc67298 |
Commercial Distribution Discontinuation | 2025-12-31 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Precision |
Version Model Number | 2650SA |
Catalog Number | 2650SA |
Company DUNS | 080935429 |
Company Name | Cardinal Health, 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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Special Storage Condition, Specify | Between 0 and 0 *; |
Special Storage Condition, Specify | Between 0 and 0 *; |
Special Storage Condition, Specify | Between 0 and 0 *; |
Special Storage Condition, Specify | Between 0 and 0 *; |
Special Storage Condition, Specify | Between 0 and 0 *; |
Special Storage Condition, Specify | Between 0 and 0 *; |
Special Storage Condition, Specify | Between 0 and 0 *; |
Special Storage Condition, Specify | Between 0 and 0 *; |
Special Storage Condition, Specify | Between 0 and 0 *; |
Special Storage Condition, Specify | Between 0 and 0 *; |
Special Storage Condition, Specify | Between 0 and 0 *; |
Special Storage Condition, Specify | Between 0 and 0 *; |
Special Storage Condition, Specify | Between 0 and 0 *; |
Special Storage Condition, Specify | Between 0 and 0 *; |
Special Storage Condition, Specify | Between 0 and 0 *; |
Special Storage Condition, Specify | Between 0 and 0 *; |
Special Storage Condition, Specify | Between 0 and 0 *; |
Special Storage Condition, Specify | Between 0 and 0 *; |