Primary Device ID | 08052440105366 |
NIH Device Record Key | 1880b61f-555a-499d-b81f-0eb3a5c99be8 |
Commercial Distribution Discontinuation | 2021-04-26 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | PressTo |
Version Model Number | PS1310 |
Catalog Number | PS1310 |
Company DUNS | 447228586 |
Company Name | MDL SRL |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
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 | 08052440105366 [Primary] |
DWO | Needle, Biopsy, Cardiovascular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-05-04 |
Device Publish Date | 2021-04-26 |
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