FDA UDI In Commercial Distribution 🇺🇸 United States

CURAPLEX

DI: 00612223260019 · Model: 301-P26000 · PEGASUS RESEARCH CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CURAPLEX
Primary DI
00612223260019
Version / Model
301-P26000
Catalog Number
P26000C
Company Name
PEGASUS RESEARCH CORPORATION
Labeler DUNS
185432994
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-09-16
Public Version
1
Public Version Date
2021-09-24
Public Version Status
New
Public Device Record Key
2099ed65-b69b-4ddf-9661-227b6cd3b806

Device Description

CURAPLEX HEATER CORE FOR 301-P2000

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
CAF Nebulizer (Direct Patient Interface)

GMDN Terms

Code Name
12050 Heated respiratory humidifier

Identifiers

Type ID
Primary 00612223260019

Premarket Submissions

Submission Number Supplement Number
K880473 000

Device Sizes

Type Value Unit Text
Height 4.5 Inch
Outer Diameter 4 Inch
Weight 1 Pound