Primary Device ID | 00840682103886 |
NIH Device Record Key | 4cf49076-9b4b-413a-b391-a47e91042ab1 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | D-lite Sensor, Disposable, Yellow |
Company DUNS | 401966697 |
Company Name | GE Healthcare Finland 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 | 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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840682103886 [Primary] |
NHO | Analyzer, gas, desflurane, gaseous-phase (anesthetic concentration) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-08-21 |
Device Publish Date | 2016-08-15 |
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