Primary Device ID | 05708265008483 |
NIH Device Record Key | 6b7f09d1-7a46-458d-b5ec-2d563098d905 |
Commercial Distribution Discontinuation | 2023-06-07 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | LiNA PowerBlade Plus™ HC |
Version Model Number | 5C-330-YH |
Company DUNS | 305088619 |
Company Name | Lina Medical ApS |
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 | 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 | 05708265008476 [Primary] |
GS1 | 05708265008483 [Package] Contains: 05708265008476 Package: box [6 Units] Discontinued: 2023-06-07 Not in Commercial Distribution |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-15 |
Device Publish Date | 2023-06-07 |
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