| Primary Device ID | 17350025911240 |
| NIH Device Record Key | b915960d-e85f-4dd3-b3be-d4c6c4f10ae2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Follicle Aspiration Set, Single Lumen |
| Version Model Number | 14125 |
| Company DUNS | 631805488 |
| Company Name | Vitrolife Sweden AB |
| 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 | false |
| 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 | 07350025911243 [Primary] |
| GS1 | 17350025911240 [Package] Contains: 07350025911243 Package: [10 Units] In Commercial Distribution |
| MQE | Needle, Assisted Reproduction |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-09 |
| 17350025914852 | 14183 |
| 17350025914241 | 14169 |
| 17350025911561 | 14157 |
| 17350025911554 | 14156 |
| 17350025911448 | 14145 |
| 17350025911387 | 14186 |
| 17350025911370 | 14185 |
| 17350025911349 | 14135 |
| 17350025911318 | 14132 |
| 17350025911295 | 14130 |
| 17350025911257 | 14126 |
| 17350025911240 | 14125 |
| 17350025911196 | 14120 |
| 17350025911189 | 14119 |
| 17350025911158 | 14116 |
| 17350025911127 | 14113 |
| 17350025911110 | 14112 |
| 17350025911066 | 14107 |
| 17350025911035 | 14104 |
| 07350025911021 | 14103 |
| 17350025911004 | 14101 |