Primary Device ID | 08800099902290 |
NIH Device Record Key | 93a842ca-d827-444e-8a86-3822766cc5e2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Perfit ZR |
Version Model Number | NA 22 A3 W |
Company DUNS | 690045351 |
Company Name | Vatechacucera, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |