Primary Device ID | 05055272700771 |
NIH Device Record Key | c113e8df-3109-43bc-825f-4fbf3736b5cd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 2.8V PROFESSIONAL OPHTH IN CASE |
Version Model Number | 1128-P-1013 |
Company DUNS | 210164398 |
Company Name | KEELER LIMITED |
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 | false |
Lot Batch | true |
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 | false |
OTC Over-The-Counter | false |