FDA UDI In Commercial Distribution 🇺🇸 United States

GLIDECATH

DI: 04987350714909 · Model: RF*ZM75115JM · TERUMO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
GLIDECATH
Primary DI
04987350714909
Version / Model
RF*ZM75115JM
Catalog Number
RF*ZM75115JM
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
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
f4b8774e-8be8-41f4-9433-a202b5eea2bb

Device Description

GLIDECATH XP

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
DQO CATHETER, INTRAVASCULAR, DIAGNOSTIC

GMDN Terms

Code Name
10688 Angiographic catheter, single-use

Identifiers

Type ID
Package 34987350714900
Primary 04987350714909
Package 54987350714904

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Hydrophilic Coating Length : 40cm
Pressure 6895 KiloPascal
Outer Diameter 1.70 Millimeter
Length 150 Centimeter
Device Size Text, specify Max Guide Wire O.D. : .038" (0.97mm)

Storage Conditions

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