Primary Device ID | 20185098000812 |
NIH Device Record Key | 71949006-b7b1-493f-95e5-bd977fb324e7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Gental Patch |
Version Model Number | ProM-027 |
Catalog Number | ProM-027 |
Company DUNS | 135741127 |
Company Name | PRO MEDICAL SUPPLIES, INC. |
Device Count | 40 |
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 | true |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
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