FDA UDI In Commercial Distribution 🇺🇸 United States

GLIDEWIRE

DI: 04987350755353 · Model: EWR5435 · TERUMO CORPORATION
Product Codes
3
GMDN Terms
2
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
GLIDEWIRE
Primary DI
04987350755353
Version / Model
EWR5435
Catalog Number
RF*GA35453E
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
3763a568-4377-447d-9297-2e15c34f2a70

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
GCJ Laparoscope, general & plastic surgery
OCY Endoscopic guidewire, gastroenterology-urology
DQX WIRE, GUIDE, CATHETER

GMDN Terms

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

Identifiers

Type ID
Package 54987350755358
Package 34987350755354
Primary 04987350755353

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Flexible Tip Length: 3cm
Length 450 Centimeter
Outer Diameter 0.89 Millimeter

Storage Conditions

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