Retrobulbar Needle - Atkinson 1123

GUDID 08134650111235

For administering local anesthetics prior to ophthalmic surgery.

HURRICANE MEDICAL INC

Hypodermic needle, single-use
Primary Device ID08134650111235
NIH Device Record Keye81b403a-6776-4cbb-bfe9-d6984e70aab6
Commercial Distribution StatusIn Commercial Distribution
Brand NameRetrobulbar Needle - Atkinson
Version Model Number1123
Catalog Number1123
Company DUNS093377724
Company NameHURRICANE MEDICAL INC
Device Count1
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Needle Gauge23 Gauge

Device Identifiers

Device Issuing AgencyDevice ID
GS108134650111235 [Primary]

FDA Product Code

GAANeedle, Aspiration And Injection, Disposable

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[08134650111235]

Ethylene Oxide;Radiation Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-01-29
Device Publish Date2020-01-21

On-Brand Devices [Retrobulbar Needle - Atkinson]

08134650111259For administering local anesthetic agents prior to ophthalmic surgery.
08134650111273Used for administering local anesthetics prior to ophthalmic surgery.
08134650111235For administering local anesthetics prior to ophthalmic surgery.
00813465010060Used for administering local anesthetics prior to ophthalmic surgery.
00813465010053For administering local anesthetic agents prior to ophthalmic surgery.
00813465010046For administering local anesthetics prior to ophthalmic surgery.

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