Primary Device ID | 00742832731539 |
NIH Device Record Key | f9747e74-c2da-47b0-9d7a-21524415a9ac |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TONOPORT BP CUFF ADULT STANDARD |
Version Model Number | 2001589-212 |
Company DUNS | 324233626 |
Company Name | PAR Medizintechnik GmbH & Co. KG |
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 | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |