| 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 |