Primary Device ID | 30817357021012 |
NIH Device Record Key | e3864cab-cdb2-4e58-9468-662a39efd7a9 |
Commercial Distribution Discontinuation | 2019-07-31 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | 3M |
Version Model Number | YMDLW5P |
Company DUNS | 177939027 |
Company Name | HYGIA HEALTH SERVICES, INC. |
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 | 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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10817357021018 [Primary] |
GS1 | 30817357021012 [Package] Contains: 10817357021018 Package: Box [25 Units] Discontinued: 2021-03-19 Not in Commercial Distribution |
IKD | Cable, Electrode |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2021-03-19 |
Device Publish Date | 2016-09-30 |
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