FDA UDI In Commercial Distribution 🇺🇸 United States

GLIDESHEATH

DI: 00389701011073 · Model: 40-1660 · TERUMO MEDICAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
GLIDESHEATH
Primary DI
00389701011073
Version / Model
40-1660
Catalog Number
40-1660
Company Name
TERUMO MEDICAL CORPORATION
Labeler DUNS
131489882
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
3
Public Version Date
2019-06-07
Public Version Status
Update
Public Device Record Key
10f01b3f-7cde-406f-9a89-e20ca7bd49fa

Device Description

GLIDESHEATH Basic Hydrophilic Coated Introducer Sheath

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
Yes
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 30389701011074
Primary 00389701011073
Package 50389701011078

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Guidewire: 0.021 Inch x 80 Centimeter Stainless Steel with Flexible Tip
Catheter Gauge 6 French
Device Size Text, specify Guidewire Compatibility: 0.021 Inch
Length 16 Centimeter

Storage Conditions

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