Primary Device ID | 10813465011972 |
NIH Device Record Key | 8c8ed63e-891c-454d-acfa-51dfdd2c41ca |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Silicone Oil Cannula |
Version Model Number | 7920 |
Catalog Number | 7920 |
Company DUNS | 093377724 |
Company Name | HURRICANE MEDICAL INC |
Device Count | 10 |
DM Exempt | true |
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 |
Needle Gauge | 20 Gauge |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00813465011975 [Primary] |
GS1 | 10813465011972 [Unit of Use] |
HMX | Cannula, Ophthalmic |
Steralize Prior To Use | true |
Device Is Sterile | true |
[10813465011972]
Radiation Sterilization;Ethylene Oxide
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-05-07 |
Device Publish Date | 2020-04-29 |
10813465011996 | Blunt tip cannula for general injection or aspiration during ophthalmic surgery. |
10813465011989 | Blunt tip cannula for general injection or aspiration during ophthalmic surgery. |
10813465011972 | Blunt tip cannula for general injection or aspiration during ophthalmic surgery. |