FDA UDI In Commercial Distribution 🇺🇸 United States

TourniKwik™

DI: 20613994576235 · Model: 79013 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
40

Basic Information

Brand Name
TourniKwik™
Primary DI
20613994576235
Version / Model
79013
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
40
Record Status
Published
Publish Date
2017-07-08
Public Version
3
Public Version Date
2021-07-08
Public Version Status
Update
Public Device Record Key
11bf4b31-5ab3-44b4-83ca-375cea550280

Device Description

TOURNIQUET 79013 TOURNIKWIK 7.5 40PK 17L

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GDJ CLAMP, SURGICAL, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
17927 Intravascular extraction catheter-snare

Identifiers

Type ID
Primary 20613994576235
Unit of Use 00613994576231

Customer Contacts

Device Sizes

Type Value Unit Text
Length 19.1 Centimeter