Primary Device ID | D742DELF1070 |
NIH Device Record Key | 4b4b0737-7a67-466c-96f2-21ee3fd675e4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Delfin1 |
Version Model Number | DELF1-07 |
Catalog Number | DELF1-07 |
Company DUNS | 131500998 |
Company Name | INTRA-LOCK INTERNATIONAL, 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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |