Primary Device ID | 06909262100104 |
NIH Device Record Key | 46166e27-05b7-4266-8fc4-5781ae32c9d2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EXTARO® 300 |
Version Model Number | 000000-2327-755 |
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 | 06909262100104 [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 |