Primary Device ID | 00040337012451 |
NIH Device Record Key | 88f41b45-a515-4f85-88b1-2d909c4b9c37 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Thermophore Deluxe |
Version Model Number | F00245 |
Company DUNS | 001957422 |
Company Name | Battle Creek Equipment Co. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
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 | 00040337002452 [Primary] |
GS1 | 00040337012451 [Package] Contains: 00040337002452 Package: Case Pack [12 Units] In Commercial Distribution |
IRT | Pad, Heating, Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-07-07 |
Device Publish Date | 2017-01-04 |
00040337012673 | Petite Thermophore Deluxe II |
00040337012666 | Medium Thermophore Deluxe II |
00040337002650 | Standard Thermophore Deluxe II |
00040337012475 | Petite Thermophore Deluxe |
00040337012468 | Medium Thermophore Deluxe |
00040337012451 | Standard Thermophore Deluxe |