FDA.reportPublic FDA data

CURAPLEX

Primary DI
612223310226
Brand
CURAPLEX
Company
PEGASUS RESEARCH CORPORATION
Model
301-P3100H-L
Catalog number
P3100HC-L
Device description
CLOSED DILUTION NEBULIZER, HIGH FLOW, UP TO 40 LPM, LONG TUBE
Published
2016-09-24
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
true

Product Codes#

Code, Name table
CodeName
CAFNebulizer (Direct Patient Interface)

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
CAFNebulizer (Direct Patient Interface)Anesthesiology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K962534000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K962534000THERA-MIST NEBULIZER MODEL-P3000Pegasus Research Corp.1997-02-28CAF

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
612223310226PackageGS140In Commercial Distribution
00612223310271PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
612223310226006122233102266122233102260612223310226
00612223310271006122233102716122233102710612223310271

GMDN Terms#

Term, Definition table
TermDefinition
Nebulizing adaptorA small connecting device, which includes an integrated nebulizer, intended to join a sterile water or sterile isotonic sodium chloride solution reservoir to a respiratory gas source (typically wall outlet) and a gas administration device (e.g., mask, mouthpiece). It is designed to generate aerosolized fluid (finely dispersed airborne droplets in a liquid phase) to be inhaled by a patient with a respiratory disorder [e.g., chronic obstructive pulmonary disease (COPD), cystic fibrosis (CF)]. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Height3.5Inch
Length16Inch
Outer Diameter2.5Inch

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
185432994
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
true
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00612223200121CURAPLEX301-P2001CFP2001CC2021-09-15
00612223057053THERMAGARD5705P20001H2016-09-23
00612223200015PEGASUSP2001P20012016-09-23
00612223200114CURAPLEX301-P2001P2001C2016-09-23
00612223060015PEGASUSP6000P60002021-09-17
00612223060510PEGASUSP6050P60502021-09-17
00612223061012PEGASUSP6100P61002021-09-17
00612223062019PEGASUSP6200P62002021-09-17
00612223062514PEGASUSP6250P62502021-09-17
00612223063016PEGASUSP6300P63002021-09-17
00612223030117CURAPLEX301-P3000NCFP3000NCC2021-09-15
00612223030131CURAPLEX301-P3000NCF-LP3000NCC-L2021-09-15
00612223030155CURAPLEX301-P3000NCF-SP3000NCC-S2021-09-15
00612223030223MISTICP3000H-CANP3000H-CAN2016-09-23
00612223030247CURAPLEX301-P3000HCFP3000HCC2021-09-15
00612223030261CURAPLEX301-P3000HCF-LP3000HCC-L2021-09-15
00612223030285CURAPLEX301-P3000HCF-SP3000HCC-S2021-09-15
00612223030339CURAPLEX301-P3000HBP3000HB2021-09-15
00612223030353CURAPLEX301-P3000CDP3000CD2021-09-15
00612223300050MISTICP3000NP3000N2016-09-23

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Primary DI, Brand, Company table
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10197344011322HUDSON RCIMEDLINE INDUSTRIES, INC.CAF2025-07-23
10197344137251HUDSON RCIMEDLINE INDUSTRIES, INC.CAF2025-05-07
10197344137244HUDSON RCIMEDLINE INDUSTRIES, INC.CAF2025-04-11
10197344006014HUDSON RCIMEDLINE INDUSTRIES, INC.CAF2025-02-21
09420012463159Fisher & Paykel HealthcareFISHER & PAYKEL HEALTHCARE LIMITEDCAF2024-08-15
10197344077564HUDSON RCIMEDLINE INDUSTRIES, INC.CAF2024-03-05
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