Primary Device ID | 00883873901045 |
NIH Device Record Key | 4edaad5d-8206-45de-adf2-2a8f7fcb9a5b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TrueCPR™ Coaching Device |
Version Model Number | 80596 |
Catalog Number | 80596-000001 |
Company DUNS | 009251992 |
Company Name | PHYSIO-CONTROL, 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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)442-1142 |
rs.seacustomersupport@physio-control.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00883873901045 [Primary] |
LIX | AID, CARDIOPULMONARY RESUSCITATION |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2014-11-11 |
00883873901045 | TRUECPR, PACKAGED, MULTI-LANGUAGE |
00883873890455 | TRUECPR,PACKAGED,MULTI-LANGUAGE, CONFIG B |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TRUECPR 85126189 4436839 Live/Registered |
Physio-Control, Inc. 2010-09-09 |