Primary Device ID | 18717872026159 |
NIH Device Record Key | b48f3339-93a0-4553-9455-fa8218ca4c8a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Backflush Instrument with 20 gauge / 0.9 mm blunt needle. |
Version Model Number | 2281.AD |
Catalog Number | 2281.AD |
Company DUNS | 407522184 |
Company Name | D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. |
Device Count | 5 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 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 |