Primary Device ID | 07540191000524 |
NIH Device Record Key | 3210eb50-a907-491d-8bf6-815ebbb95921 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GSR2 Unit Protected Pin |
Version Model Number | SA2000M |
Company DUNS | 209284132 |
Company Name | Technologie de Pensée Ltée |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
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 | 07540191000524 [Primary] |
HCC | Device, Biofeedback |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-11-20 |
Device Publish Date | 2019-10-29 |
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