Primary Device ID | 14048223016821 |
NIH Device Record Key | 1d104caf-bbb9-4ff9-8f49-c178b3ff5809 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Coaxial sleeve Ø 1,50 (17G) |
Version Model Number | 413S150112 |
Catalog Number | 413S150112 |
Company DUNS | 317654283 |
Company Name | Pajunk GmbH Medizintechnologie |
Device Count | 10 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(888)972-5865 |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 04048223016824 [Unit of Use] |
GS1 | 14048223016821 [Primary] |
MJG | DEVICE, PERCUTANEOUS, BIOPSY |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-10-07 |
Device Publish Date | 2016-12-15 |
14048223016838 | Coaxial sleeve Ø 1,50 (17G) for PrimoCut Ø 1,20 (18G)x 200,sterile |
14048223016821 | Coaxial sleeve Ø 1,50 (17G) for PrimoCut Ø 1,20 (18G)x 150,sterile |