| Primary Device ID | 00810563020113 |
| NIH Device Record Key | 85957465-baae-4290-aae9-b80a15818de5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TempProbe™ |
| Version Model Number | CRYO-54-F |
| Catalog Number | CRYO-54-F |
| 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 | 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 | true |
| OTC Over-The-Counter | false |
| Phone | 5123282892 |
| xx@xx.xx | |
| Phone | 5123282892 |
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| Phone | 5123282892 |
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| Phone | 5123282892 |
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| Phone | 5123282892 |
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| Phone | 5123282892 |
| xx@xx.xx | |
| Phone | 5123282892 |
| xx@xx.xx | |
| Phone | 5123282892 |
| xx@xx.xx | |
| Phone | 5123282892 |
| xx@xx.xx | |
| Phone | 5123282892 |
| xx@xx.xx | |
| Phone | 5123282892 |
| xx@xx.xx | |
| Phone | 5123282892 |
| xx@xx.xx | |
| Phone | 5123282892 |
| xx@xx.xx | |
| Phone | 5123282892 |
| xx@xx.xx | |
| Phone | 5123282892 |
| xx@xx.xx | |
| Phone | 5123282892 |
| xx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810563020113 [Primary] |
| GEH | Unit, Cryosurgical, Accessories |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-07-31 |
| 00810563020120 | Endocare™ TempProbe™ Device |
| 00810563020113 | Endocare™ TempProbe™ Device |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() TEMPPROBE 78024764 2580369 Live/Registered |
Endocare, Inc. 2000-09-07 |