| Primary Device ID | 04059082005522 |
| NIH Device Record Key | 1fc6ebcf-811e-4035-a8b1-633c2d206826 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Trocar sleeve |
| Version Model Number | 191 120 120 |
| Company DUNS | 507185952 |
| Company Name | SOPRO-COMEG GmbH |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 | 04059082005522 [Primary] |
| GCJ | Laparoscope, general & plastic surgery |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04059082005522]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-12 |
| 04059082005522 | 191 120 120 |
| 04059082005508 | 191 120 090 |
| 04059082005492 | 191 120 080 |
| 04059082005485 | 191 120 070 |
| 04059082005362 | 191 111 110 |
| 04059082005355 | 191 111 100 |
| 04059082005348 | 191 111 090 |
| 04059082005331 | 191 111 080 |
| 04059082005324 | 191 111 070 |
| 04059082005218 | 191 101 080 |
| 04059082005201 | 191 101 070 |
| 04059082005089 | 191 070 080 |
| 04059082004914 | 191 051 120 |
| 04059082004907 | 191 051 110 |
| 04059082004891 | 191 051 100 |
| 04059082004884 | 191 051 090 |
| 04059082004877 | 191 051 080 |
| 04059082004860 | 191 051 070 |
| 04059082004785 | 191 031 080 |
| 04059082004778 | 191 031 070 |