Primary Device ID | 00768627001755 |
NIH Device Record Key | 751f63e5-5e2c-4dea-800b-6ea92c0e4194 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Norco Iontophoresis Large Sample |
Version Model Number | SA89252B |
Company DUNS | 060121928 |
Company Name | NORTH COAST MEDICAL, 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 | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00768627001755 [Primary] |
EGJ | Device, Iontophoresis, Other Uses |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-07-01 |
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