Primary Device ID | 00849405021223 |
NIH Device Record Key | ff4e4497-d812-4f76-97d2-623c1ae3cd64 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Foam Kit Thin Medium |
Version Model Number | XF-DMDF1-T |
Company DUNS | 006616130 |
Company Name | GENADYNE BIOTECHNOLOGIES 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 | true |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00849405021223 [Primary] |
OMP | Negative Pressure Wound Therapy Powered Suction Pump |
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 | 2016-09-24 |
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