| Primary Device ID | 00810563020373 | 
| NIH Device Record Key | db74196a-736a-4403-a28b-93d929f1e2e3 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Cryocare CS™ | 
| Version Model Number | CRYO-CS-3 Version 5 | 
| Catalog Number | CRYO-CS-3 Version 4 | 
| Company DUNS | 928955509 | 
| Company Name | ENDOCARE, INC. | 
| 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 | 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 | 
| Phone | 5123282892 | 
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| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00810563020373 [Primary] | 
| GEH | Unit, Cryosurgical, Accessories | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 3 | 
| Public Version Date | 2018-07-06 | 
| Device Publish Date | 2016-07-31 | 
| 00810563020519 | Endocare™ Cryocare CS™ System Version 5 | 
| 00810563020502 | Endocare™ Cryocare CS™ System Basic | 
| 00810563020410 | Endocare™ Cryocare CS™ System Basic | 
| 00810563020373 | Endocare™ Cryocare CS™ System Version 5 | 
| 00810563020366 | Endocare™ Cryocare CS™ System Version 4 | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  CRYOCARE CS  78767012  3309240 Live/Registered | Endocare, Inc. 2005-12-05 | 
|  CRYOCARE CS  78766988  3309239 Live/Registered | Endocare, Inc. 2005-12-05 |