| Primary Device ID | 07613327063905 | 
| NIH Device Record Key | 106828de-3819-45a9-9900-978b43ae0b06 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | AIM (Advanced Imaging Modality) | 
| Version Model Number | 0502937010 | 
| Catalog Number | 0502-937-010 | 
| Company DUNS | 187502109 | 
| Company Name | STRYKER CORPORATION | 
| 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 | false | 
| Serial Number | true | 
| Manufacturing Date | false | 
| 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 | 
| Phone | +1(866)624-4422 | 
| xx@xx.xx | 
| Device Size Text, specify | 0 | 
| Length | 33 Centimeter | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 07613327063905 [Primary] | 
| OWN | Confocal optical imaging | 
| Steralize Prior To Use | true | 
| Device Is Sterile | false | 
[07613327063905]
Ethylene Oxide;Moist Heat or Steam Sterilization;Hydrogen Peroxide
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 3 | 
| Public Version Date | 2018-07-06 | 
| Device Publish Date | 2016-09-23 | 
| 07613327063912 | HD Laparoscope, Autoclavable, 30 ¿ View Direction | 
| 07613327063905 | HD Laparoscope, Autoclavable, 0 ¿ View Direction | 
| 07613327059373 | HD Laparoscope, Autoclavable, 30 ¿ View Direction | 
| 07613327059342 | HD Laparoscope, Autoclavable, 0 ¿ View Direction |