Primary Device ID | 08134650111235 |
NIH Device Record Key | e81b403a-6776-4cbb-bfe9-d6984e70aab6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Retrobulbar Needle - Atkinson |
Version Model Number | 1123 |
Catalog Number | 1123 |
Company DUNS | 093377724 |
Company Name | HURRICANE MEDICAL INC |
Device Count | 1 |
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 | 23 Gauge |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08134650111235 [Primary] |
GAA | Needle, Aspiration And Injection, Disposable |
Steralize Prior To Use | true |
Device Is Sterile | true |
[08134650111235]
Ethylene Oxide;Radiation Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-01-29 |
Device Publish Date | 2020-01-21 |
08134650111259 | For administering local anesthetic agents prior to ophthalmic surgery. |
08134650111273 | Used for administering local anesthetics prior to ophthalmic surgery. |
08134650111235 | For administering local anesthetics prior to ophthalmic surgery. |
00813465010060 | Used for administering local anesthetics prior to ophthalmic surgery. |
00813465010053 | For administering local anesthetic agents prior to ophthalmic surgery. |
00813465010046 | For administering local anesthetics prior to ophthalmic surgery. |