Primary Device ID | 06900234100207 |
NIH Device Record Key | 11e35a0c-ea04-47ae-a65d-841971cca3d3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Solaris |
Version Model Number | T100P-090087 |
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 | 06900234100207 [Primary] |
GS1 | 16900234100204 [Package] Contains: 56900234100202 Package: Box [20 Units] In Commercial Distribution |
GS1 | 26900234100201 [Package] Contains: 56900234100202 Package: Box [32 Units] In Commercial Distribution |
GS1 | 36900234100208 [Package] Contains: 56900234100202 Package: Box [40 Units] In Commercial Distribution |
GS1 | 46900234100205 [Package] Contains: 56900234100202 Package: Box [60 Units] In Commercial Distribution |
GS1 | 56900234100202 [Package] Package: Box [80 Units] In Commercial Distribution |
DQA | Oximeter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-01-17 |
Device Publish Date | 2020-01-09 |
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