Primary Device ID | 10190752103733 |
NIH Device Record Key | 6b5361ba-6b55-4b53-bb3c-0f11232aa122 |
Commercial Distribution Discontinuation | 2022-03-31 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Vital Signs™ |
Version Model Number | 2089797-002 |
Catalog Number | 2089797-002 |
Company DUNS | 367919120 |
Company Name | Carefusion Finland 320 Oy |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10190752103733 [Primary] |
DSA | Cable, Transducer And Electrode, Patient, (Including Connector) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2024-05-27 |
Device Publish Date | 2017-08-01 |
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