| Primary Device ID | 17350025915699 |
| NIH Device Record Key | d17cfb66-7030-4c94-b8b2-337499ad526e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Follicle Aspiration Set Single Lumen |
| Version Model Number | 17189 |
| 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 | 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 | 07350025915692 [Primary] |
| GS1 | 17350025915699 [Package] Contains: 07350025915692 Package: [10 Units] In Commercial Distribution |
| MQE | Needle, Assisted Reproduction |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-07-10 |
| Device Publish Date | 2024-07-02 |
| 17350025915514 | 17186 |
| 17350025915507 | 17185 |
| 17350025915491 | 17183 |
| 17350025915385 | 17157 |
| 17350025915378 | 17156 |
| 17350025915309 | 17145 |
| 17350025915262 | 17132 |
| 17350025915248 | 17130 |
| 17350025915224 | 17126 |
| 17350025915217 | 17125 |
| 17350025915194 | 17120 |
| 17350025915187 | 17119 |
| 17350025915170 | 17116 |
| 17350025915156 | 17113 |
| 17350025915149 | 17112 |
| 17350025915101 | 17107 |
| 17350025915088 | 17104 |
| 17350025915071 | 17103 |
| 17350025915699 | 17189 |