Primary Device ID | 00840178700100 |
NIH Device Record Key | 6ae1dd6e-387d-40e4-a612-d3e8c4a15307 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PROCARE |
Version Model Number | 120-002407-00 |
Company DUNS | 080434935 |
Company Name | Touchpoint Medical, Inc. |
Device Count | 1 |
DM Exempt | true |
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 | false |
Serial Number | true |
Manufacturing Date | true |
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 | 00840178700100 [Primary] |
BZN | Cart, Emergency, Cardiopulmonary (Excluding Equipment) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-04-09 |
Device Publish Date | 2024-04-01 |
00840178700100 | ProCare Intelligent Anesthesia Cart |
00840178700094 | ProCare Intelligent Procedure Cart |
00840178700087 | ProCare Anesthesia Cart |
00840178700070 | ProCare Pediatric Code Response Cart |
00840178700063 | ProCare Emergency Code Response Cart |
00840178700056 | ProCare General Procedure Cart, E-Lock |
00840178700049 | ProCare General Procedure Cart |
00840178700032 | ProCare Isolation Cart |