FDA UDI In Commercial Distribution 🇺🇸 United States

transGlide Expandable Introducer

DI: 00866697000200 · Model: 16F transGlide Expandable Introducer · TRANS AORTIC MEDICAL INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
transGlide Expandable Introducer
Primary DI
00866697000200
Version / Model
16F transGlide Expandable Introducer
Catalog Number
TA-004
Company Name
TRANS AORTIC MEDICAL INC
Labeler DUNS
071067163
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-01
Public Version
4
Public Version Date
2019-06-07
Public Version Status
Update
Public Device Record Key
9b81a326-07ec-4282-9588-e6abc8d4b8aa

Device Description

16F transGlide Expandable Introducer

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
Primary 00866697000200

Customer Contacts

Phone
4087794200
Phone
4087794200

Premarket Submissions

Submission Number Supplement Number
K152194 000

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 5.3 Millimeter