Primary Device ID | 00816703021323 |
NIH Device Record Key | d145c876-4b63-489f-a9d8-33d0e10e739d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MedSource Electrode (4/pk - 150pk/cs ) |
Version Model Number | MS-65004 |
Company DUNS | 041674552 |
Company Name | MEDSOURCE INTERNATIONAL LLC |
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 | true |
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 | 00816703021323 [Primary] |
DRX | Electrode, Electrocardiograph |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-07-14 |
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