FDA UDI In Commercial Distribution 🇺🇸 United States

DLP®

DI: 20613994576402 · Model: 79005 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
40

Basic Information

Brand Name
DLP®
Primary DI
20613994576402
Version / Model
79005
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
1d55dddf-f246-4c43-a705-a04227386ae1

Device Description

TOURNIQUET 79005 VENA CAVA 7IN 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 20613994576402
Unit of Use 00613994576408

Customer Contacts

Device Sizes

Type Value Unit Text
Length 17.8 Centimeter