FDA UDI In Commercial Distribution 🇺🇸 United States

DLP®

DI: 20643169880959 · Model: 61000 · MEDTRONIC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
DLP®
Primary DI
20643169880959
Version / Model
61000
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2019-03-03
Public Version
2
Public Version Date
2022-12-08
Public Version Status
Update
Public Device Record Key
18d44edc-4e06-4b08-ab41-1083fdd0bc15

Device Description

PRESSURE DISPLAY SET W/STOPCOCK 45 INCH

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
No
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
FMH CONTAINER, SPECIMEN, STERILE
DXS GAUGE, PRESSURE, CORONARY, CARDIOPULMONARY BYPASS

GMDN Terms

Code Name
35441 Cardiopulmonary bypass system blood tubing set

Identifiers

Type ID
Primary 20643169880959
Unit of Use 00643169880955

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K113235 000

Device Sizes

Type Value Unit Text
Length 114.3 Centimeter