FDA UDI In Commercial Distribution 🇺🇸 United States

RUNTHROUGH

DI: 04987350734709 · Model: 25-5211 · TERUMO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
RUNTHROUGH
Primary DI
04987350734709
Version / Model
25-5211
Catalog Number
TW*AS418XHW
Company Name
TERUMO CORPORATION
Labeler DUNS
690543319
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-09
Public Version
1
Public Version Date
2022-09-19
Public Version Status
New
Public Device Record Key
0ed44ba8-cf37-4670-96b1-f0a04a78481d

Device Description

RUNTHROUGH NS Izanai PTCA Guidewire

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Unsafe
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

GMDN Terms

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

Identifiers

Type ID
Package 34987350734700
Primary 04987350734709
Package 54987350734704

Customer Contacts

Device Sizes

Type Value Unit Text
Length 180 Centimeter
Device Size Text, specify Radiopaque Length: 3cm
Outer Diameter 0.36 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Fragile. Keep dry. Keep away from sunlight. Stacking limit by 10.