FDA.reportPublic FDA data

AURORA®

Primary DI
00850002332209
Brand
AURORA®
Company
REBOUND THERAPEUTICS CORPORATION
Model
AEC12F/130
Catalog number
AEC12F/130
Device description
AURORA® Evacuator +Coag 12F (4.0mm), Length: 130mm
Published
2021-01-12
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
GEIElectrosurgical, Cutting & Coagulation & Accessories

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GEIElectrosurgical, Cutting & Coagulation & AccessoriesGeneral, Plastic Surgery2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K201637000
K203745000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K201637000Aurora Evacuator +CoagRebound Therapeutics2020-08-12GEI
K203745000AURORA Evacuator +CoagRebound Therapeutics2021-12-02GEI

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00850002332209PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00850002332209008500023322098500023322090850002332209

GMDN Terms#

Term, Definition table
TermDefinition
General-purpose surgical suction system, vacuumAn assembly of vacuum-powered devices, which includes a surgically invasive component, designed to aspirate unwanted materials (e.g., debris, tissues, fluids) from body cavities/wounds during a surgical procedure (e.g., general surgery, laparoscopy); it may in addition have non-surgical applications. It is connected via dedicated tubing to the terminal unit (wall outlet) of a vacuum pipeline system and relies on the healthcare facility’s central vacuum system. It includes a vacuum suction regulator which controls negative pressure for the aspiration, collection containers, and patient contact devices (e.g., handpiece/tip); it typically also includes tubing and microbial/hydrophobic filters.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Length130Millimeter
Outer Diameter4Millimeter

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Handling Environment Atmospheric Pressure500 millibar1050 millibar
Handling Environment Humidity15 Percent (%) Relative Humidity85 Percent (%) Relative Humidity
Handling Environment Temperature-10 Degrees Celsius60 Degrees Celsius
Handling Environment Temperature14 Degrees Fahrenheit140 Degrees Fahrenheit
Special Storage Condition, Specify00Keep Dry, Keep away from sunlight, Do Not Use if Package is Damaged
Storage Environment Humidity15 Percent (%) Relative Humidity85 Percent (%) Relative Humidity
Storage Environment Temperature-10 Degrees Celsius60 Degrees Celsius
Storage Environment Temperature14 Degrees Fahrenheit140 Degrees Fahrenheit

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(800)654-2873custsvcnj@integralife.com

Regulatory Flags#

DUNS number
080909607
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00850002332049AURORA® Surgiscope®ICB/PCICB/PC2022-11-29
00850002332223AURORA®AEC12F/70AEC12F/702021-01-12
00850002332216AURORA®AEC12F/100AEC12F/1002021-01-12
00850002332148AURORA®AE10F/130AE10F/1302020-02-06
00850002332155AURORA®AE10F/100AE10F/1002020-02-06
00850002332162AURORA®AE10F/70AE10F/702020-02-06
00860624000400AURORA® Surgiscope®Image Control BoxIMAGE_CONTROL_BOX2019-01-22
00850002332131AURORA® Surgiscope®AS8/130AS8/1302019-12-18
00860624000455AURORA® Surgiscope®AS8/100AS8/1002019-12-18
00860624000462AURORA® Surgiscope®AS8/70AS8/702019-12-18
00860624000448AURORA SurgiscopeAURORA Surgiscope-13AURORA Surgiscope-132019-01-22
00850002332001AURORA EvacuatorAURORA Evacuator-10Fx13cmAURORA Evacuator-10Fx13cm2019-04-30
00850002332063AURORA EvacuatorAURORA Evacuator-9Fx13cmAURORA Evacuator-9Fx13cm2019-04-30
00850002332070AURORA EvacuatorAURORA Evacuator-9Fx10cmAURORA Evacuator-9Fx10cm2019-04-30
00860624000417AURORA EvacuatorAURORA Evacuator-13AURORA Evacuator-132018-05-29
00850002332018AURORA EvacuatorAURORA Evacuator-10Fx10cmAURORA Evacuator-10Fx10cm2019-04-30
00850002332025AURORA EvacuatorAURORA Evacuator-10Fx7cmAURORA Evacuator-10Fx7cm2019-04-30
00850002332087AURORA EvacuatorAURORA Evacuator-9Fx7cmAURORA Evacuator-9Fx7cm2019-04-30
00860624000424AURORA EvacuatorAURORA Evacuator-10AURORA Evacuator-102018-05-29
00860624000431AURORA EvacuatorAURORA Evacuator-7AURORA Evacuator-72018-05-29

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00197998302718Solventum™Solventum US LLCGEI2026-09-25
00724995269586Snowden-PencerSTERIS Deutschland GmbHGEI2026-09-25
00724995269951Snowden-PencerSTERIS Deutschland GmbHGEI2026-09-25
00724995269968Snowden-PencerSTERIS Deutschland GmbHGEI2026-09-25
00190776432300MillenniumAvalign Technologies, Inc.GEI2026-09-24
00190776432317MillenniumAvalign Technologies, Inc.GEI2026-09-24
00190776432324MillenniumAvalign Technologies, Inc.GEI2026-09-24
00190776432430MillenniumAvalign Technologies, Inc.GEI2026-09-24
00190776432447MillenniumAvalign Technologies, Inc.GEI2026-09-24
00190776432454MillenniumAvalign Technologies, Inc.GEI2026-09-24
00190776431457MillenniumAvalign Technologies, Inc.GEI2026-09-22
00190776432041MillenniumAvalign Technologies, Inc.GEI2026-09-22
00190776432195MillenniumAvalign Technologies, Inc.GEI2026-09-22
00190776432201MillenniumAvalign Technologies, Inc.GEI2026-09-22
00190776431181MillenniumAvalign Technologies, Inc.GEI2026-09-21
00190776431198MillenniumAvalign Technologies, Inc.GEI2026-09-21
00190776431204MillenniumAvalign Technologies, Inc.GEI2026-09-21
00190776431211MillenniumAvalign Technologies, Inc.GEI2026-09-21
00190776431228MillenniumAvalign Technologies, Inc.GEI2026-09-21
00190776431235MillenniumAvalign Technologies, Inc.GEI2026-09-21
00190776431242MillenniumAvalign Technologies, Inc.GEI2026-09-21
00190776431259MillenniumAvalign Technologies, Inc.GEI2026-09-21
10840113236852BovieASPEN SURGICAL PRODUCTS, INC.GEI2026-09-21
10840113236890BovieASPEN SURGICAL PRODUCTS, INC.GEI2026-09-21
10840113236937BovieASPEN SURGICAL PRODUCTS, INC.GEI2026-09-21
10840113237040BovieASPEN SURGICAL PRODUCTS, INC.GEI2026-09-21
10840113237064BovieASPEN SURGICAL PRODUCTS, INC.GEI2026-09-21
10840113237101BovieASPEN SURGICAL PRODUCTS, INC.GEI2026-09-21
10840113237118BovieASPEN SURGICAL PRODUCTS, INC.GEI2026-09-21
10840113237132BovieASPEN SURGICAL PRODUCTS, INC.GEI2026-09-21