Primary Device ID | 04260671372219 |
NIH Device Record Key | 6b2aa69b-fa62-45b0-9cd8-7e3d902d2bb8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TONOPORT BP Single-Use Cuff for Adults, Standard |
Version Model Number | 2001589-233 |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |