Primary Device ID | 08717872009155 |
NIH Device Record Key | 9e7f662f-60b4-43f1-a305-417014e88064 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Phaco fragmentation needle, titanium.(20 gauge / 0.9 mm) |
Version Model Number | 3005.FT |
Catalog Number | 3005.FT |
Company DUNS | 407522184 |
Company Name | D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. |
Device Count | 3 |
DM Exempt | true |
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 | false |
Lot Batch | false |
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 | true |
OTC Over-The-Counter | false |