Primary Device ID | 30020451458930 |
NIH Device Record Key | 17562b5e-5767-4ecf-92c0-5a132e976805 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Invia Motion 15 Days Kit 10 x 25 cm |
Version Model Number | 101045893 |
Company DUNS | 488293218 |
Company Name | Medela AG |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 30020451458930 [Primary] |
OMP | Negative Pressure Wound Therapy Powered Suction Pump |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-09-11 |
Device Publish Date | 2023-09-01 |
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