FDA UDI In Commercial Distribution 🇺🇸 United States

RevoWave™

DI: 04545428038700 · Model: RWHA-2526ID · PIOLAX MEDICAL DEVICES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
RevoWave™
Primary DI
04545428038700
Version / Model
RWHA-2526ID
Catalog Number
RWHA-2526ID
Company Name
PIOLAX MEDICAL DEVICES, INC.
Labeler DUNS
693961984
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-22
Public Version
1
Public Version Date
2019-04-01
Public Version Status
New
Public Device Record Key
4d84c431-f329-4d9a-b148-605530a282e8

Device Description

0.025 Hard

Device Characteristics

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OCY Endoscopic Guidewire, Gastroenterology-Urology

GMDN Terms

Code Name
46691 Gastro-urological guidewire, single-use

Identifiers

Type ID
Package 14545428038707
Primary 04545428038700

Device Sizes

Type Value Unit Text
Device Size Text, specify Adaptable type : 0.025 inch
Length 260 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Avoid exposure to high temperature, high humidity, direct sunlight, ultraviolet light (from germicidal lamp, etc.) and water during storage.