Primary Device ID | D724DELF1020 |
NIH Device Record Key | a861881b-8d44-4775-b0e7-993e9fae5a43 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Delfin1 |
Version Model Number | DELF1-02 |
Catalog Number | DELF1-02 |
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 |