FDA UDI In Commercial Distribution 🇺🇸 United States

GLIDEWIRE

DI: 04987350755759 · Model: EWS4035 · TERUMO CORPORATION
Product Codes
3
GMDN Terms
2
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
GLIDEWIRE
Primary DI
04987350755759
Version / Model
EWS4035
Catalog Number
RF*PS35263E
Company Name
TERUMO CORPORATION
Labeler DUNS
690543319
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-09
Public Version
4
Public Version Date
2022-08-23
Public Version Status
Update
Public Device Record Key
04b51853-4e2e-4252-bd66-cb5499989b63

Device Description

RADIFOCUS GLIDEWIRE

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
No
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
DQX WIRE, GUIDE, CATHETER
GCJ Laparoscope, general & plastic surgery
OCY Endoscopic guidewire, gastroenterology-urology

GMDN Terms

Code Name
46691 Gastro-urological guidewire, single-use
35094 Cardiac/peripheral vascular guidewire, single-use

Identifiers

Type ID
Package 54987350755754
Package 34987350755750
Primary 04987350755759

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 0.89 Millimeter
Device Size Text, specify Flexible Tip Length: 3cm
Length 260 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Fragile.Keep away from rain. Keep away from sunlight.