Primary Device ID | 04250413410132 |
NIH Device Record Key | 4958ea48-35c0-4004-aeb8-31ab3b979a53 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Inductive Effort Belt for SOMNO HD (Abdomen) - si |
Version Model Number | NGA203 |
Company DUNS | 314112173 |
Company Name | SOMNOmedics GmbH |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04250413410132 [Primary] |
MNR | Ventilatory Effort Recorder |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-12-17 |
Device Publish Date | 2018-11-16 |
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