Primary Device ID | 00817377023088 |
NIH Device Record Key | 2e5ee2dd-fb1e-4b4d-ad6e-737f43cba1c3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Precision Gold |
Version Model Number | 13-10200-4010 |
Company DUNS | 079976463 |
Company Name | DYMEDIX DIAGNOSTICS, 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 | true |
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 | 00817377023088 [Primary] |
GXY | Electrode, Cutaneous |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-07-09 |
Device Publish Date | 2021-07-01 |
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Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PRECISION GOLD 76231449 not registered Dead/Abandoned |
PNY Technologies, Inc. 2001-03-27 |
PRECISION GOLD 73832810 1831430 Dead/Cancelled |
STRIKER GOLF COMPANY 1989-10-23 |