| Primary Device ID | 00810563020908 | 
| NIH Device Record Key | 4753f763-18f6-4eeb-9c24-988fdd1cb98c | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | TempProbe™ Device | 
| Version Model Number | DP40-0015-213 | 
| Catalog Number | CRYO-55-F | 
| Company DUNS | 009120817 | 
| Company Name | VARIAN MEDICAL SYSTEMS, INC. | 
| Device Count | 1 | 
| DM Exempt | false | 
| Pre-market Exempt | false | 
| MRI Safety Status | MR Unsafe | 
| Human Cell/Tissue Product | false | 
| Device Kit | false | 
| Device Combination Product | false | 
| Single Use | true | 
| Lot Batch | true | 
| Serial Number | false | 
| Manufacturing Date | true | 
| Expiration Date | true | 
| 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 | 00810563020908 [Primary] | 
| GEH | UNIT, CRYOSURGICAL, ACCESSORIES | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2022-02-28 | 
| Device Publish Date | 2022-02-18 | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  TEMPPROBE  78024764  2580369 Live/Registered | Endocare, Inc. 2000-09-07 |