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 |
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 | |
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 |