| Primary Device ID | 15420045505094 |
| NIH Device Record Key | 75ffa581-fa1e-4766-aa86-de1744594e29 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MyoSure Tissue Removal Device |
| Version Model Number | 50-501XL |
| Catalog Number | 50-501XL |
| Company DUNS | 018925968 |
| Company Name | Hologic, Inc. |
| Device Count | 1 |
| DM Exempt | true |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 15420045505094 [Primary] |
| GS1 | 25420045505091 [Package] Package: CARTON [1 Units] In Commercial Distribution |
| GS1 | 35420045505098 [Package] Contains: 25420045505091 Package: BOX [3 Units] In Commercial Distribution |
| HIH | HYSTEROSCOPE (AND ACCESSORIES) |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[15420045505094]
Ethylene Oxide
[15420045505094]
Ethylene Oxide
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-08-08 |
| 25420045505107 | 40-902 |
| 15420045505094 | 50-501XL |
| 15420045505087 | 50-401XL |
| 15420045505070 | 30-401LITE |
| 15420045504813 | 10-401 |