FDA UDI In Commercial Distribution 🇺🇸 United States

GLIDESHEATH SLENDER

DI: 00389701011950 · Model: 60-1050 · TERUMO MEDICAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
GLIDESHEATH SLENDER
Primary DI
00389701011950
Version / Model
60-1050
Catalog Number
60-1050
Company Name
TERUMO MEDICAL CORPORATION
Labeler DUNS
131489882
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-23
Public Version
2
Public Version Date
2019-06-07
Public Version Status
Update
Public Device Record Key
aa603135-c3bc-4e5e-86b9-15eb5f0c017a

Device Description

GLIDESHEATH SLENDER Access Kit

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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
DYB INTRODUCER, CATHETER

GMDN Terms

Code Name
58865 Vascular catheter introduction set, nonimplantable

Identifiers

Type ID
Package 50389701011955
Package 30389701011951
Primary 00389701011950

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Needle: 22 Gauge x 0.984" (25 mm)
Device Size Text, specify Guidewire: 0.021 Inch x 45 cm Plastic Jacketed Shortangle
Length 10 Centimeter
Catheter Gauge 5 French

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Avoid direct sunlight. Keep Dry.
Type
Special Storage Condition, Specify
Special Conditions
Do not store at extreme temperature and humidity