| Primary Device ID | 06909262060330 |
| NIH Device Record Key | f50630c8-c565-4986-8020-3a4f7a62e0b6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | EXTARO® 300 |
| Version Model Number | 6033 |
| Company DUNS | 528182577 |
| Company Name | Carl Zeiss Suzhou Co., Ltd. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Conditional |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| 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 | 06909262060330 [Primary] |
| EPT | Microscope, Surgical |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-08-19 |
| Device Publish Date | 2022-08-11 |
| 06909262100104 | 000000-2327-755 |
| 06909262060354 | 6035 |
| 06909262060347 | 6034 |
| 06909262060330 | 6033 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() EXTARO 87134097 5263811 Live/Registered |
Carl Zeiss Meditec AG 2016-08-10 |