| Primary Device ID | 14048223016838 |
| NIH Device Record Key | dc335770-07ee-4e94-a46e-016c3b7c2dee |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Coaxial sleeve Ø 1,50 (17G) |
| Version Model Number | 413S150162 |
| Catalog Number | 413S150162 |
| 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 |
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| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04048223016831 [Unit of Use] |
| GS1 | 14048223016838 [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 |
| 04048223131923 | Coaxial sleeve Ø 1,50 (17G) for PrimoCut Ø 1,20 (18G)x 150,sterile |
| 04048223128947 | Coaxial sleeve Ø 1,50 (17G) for PrimoCut Ø 1,20 (18G)x 200,sterile |