Primary Device ID | 00681490595896 |
NIH Device Record Key | 01de674a-ec55-4a0d-bcca-52dba425ed86 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 50mm x 22m ECG Printer Paper (3/roll) |
Version Model Number | 11240 |
Catalog Number | 11240-000013 |
Company DUNS | 009251992 |
Company Name | PHYSIO-CONTROL, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | +1(800)442-1142 |
rs.seacustomersupport@physio-control.com | |
Phone | +1(800)442-1142 |
rs.seacustomersupport@physio-control.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00681490595896 [Primary] |
DSF | RECORDER, PAPER CHART |
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 | 2016-09-17 |
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