Fenestrated Atraumatic Forceps Inner Shaft C279

GUDID B354C2790

Fenestrated Atraumatic Forceps Inner Shaft

ORANGE SURGICAL INSTRUMENTS, LLC

Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use
Primary Device IDB354C2790
NIH Device Record Key829f903b-0198-4731-8811-8b44df1981bd
Commercial Distribution Discontinuation2022-05-01
Commercial Distribution StatusIn Commercial Distribution
Brand NameFenestrated Atraumatic Forceps Inner Shaft
Version Model NumberC279
Catalog NumberC279
Company DUNS047063695
Company NameORANGE SURGICAL INSTRUMENTS, LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB354C2790 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIElectrosurgical, Cutting & Coagulation & Accessories

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


[B354C2790]

Peracetic Acid


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-05-09
Device Publish Date2019-05-01

On-Brand Devices [Fenestrated Atraumatic Forceps Inner Shaft]

B354279Fenestrated Atraumatic Forceps Inner Shaft
B354C2790Fenestrated Atraumatic Forceps Inner Shaft

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