Primary Device ID | 00884838099128 |
NIH Device Record Key | 6b1bb35e-7cf5-459f-863b-7ea6beb742bb |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | C |
Company DUNS | 078628040 |
Company Name | Philips Medical Systems |
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 | false |
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 | false |
Phone | +1(999)999-9999 |
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Phone | +1(999)999-9999 |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 00884838099128 [Primary] |
MSX | System, network and communication, physiological monitors |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-12-03 |
Device Publish Date | 2019-11-25 |