FDA UDI In Commercial Distribution 🇺🇸 United States

DLP®

DI: 20613994846666 · Model: 62006 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
DLP®
Primary DI
20613994846666
Version / Model
62006
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2016-06-13
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
c6b61142-c4be-49f1-8d9b-bc56b870995b

Device Description

SET 62006 PRESSURE DISPLAY 72 5PK 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
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
DXS GAUGE, PRESSURE, CORONARY, CARDIOPULMONARY BYPASS

GMDN Terms

Code Name
36550 Patient monitoring system module, blood pressure, invasive

Identifiers

Type ID
Primary 20613994846666
Unit of Use 00613994846662

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K852232 000

Device Sizes

Type Value Unit Text
Length 182.9 Centimeter