Primary Device ID | D7700634813 |
NIH Device Record Key | 3c80b91f-3c13-470f-b616-854a8a26b279 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PULL-UP TRANSFER FOR PRE-KOH |
Version Model Number | A-TRARP-380 |
Catalog Number | A-TRARP-380 |
Company DUNS | 433815198 |
Company Name | SWEDEN & MARTINA SPA |
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 | true |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |