Primary Device ID | 56900234100097 |
NIH Device Record Key | 30c41114-b7fc-400d-9543-5f2d1acfc2f7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Solaris |
Version Model Number | S100A-090110 |
Company DUNS | 527945351 |
Company Name | Solaris Medical Technology, Inc. |
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 | true |
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 | 06900234100092 [Primary] |
GS1 | 16900234100099 [Package] Contains: 06900234100092 Package: [20 Units] In Commercial Distribution |
GS1 | 26900234100096 [Package] Contains: 06900234100092 Package: [32 Units] In Commercial Distribution |
GS1 | 36900234100093 [Package] Contains: 06900234100092 Package: [40 Units] In Commercial Distribution |
GS1 | 46900234100090 [Package] Contains: 06900234100092 Package: [60 Units] In Commercial Distribution |
GS1 | 56900234100097 [Package] Contains: 06900234100092 Package: [80 Units] In Commercial Distribution |
DQA | Oximeter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-01-09 |
Device Publish Date | 2016-12-30 |
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