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 |