FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00613994258120 · Model: BD38 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00613994258120
Version / Model
BD38
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-18
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
9d9a10a4-a011-4f63-9915-b86f2f9e8a17

Device Description

DETECTOR BD38 BUBBLE ADULT

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
No
Sterilization Prior Use
No

Product Codes

Code Name
DWA Control, pump speed, cardiopulmonary bypass

GMDN Terms

Code Name
35440 Cardiopulmonary bypass system air bubble/fluid level detector

Identifiers

Type ID
Primary 00613994258120

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K070286 000

Storage Conditions

Type
Storage Environment Atmospheric Pressure
Temperature Range
700 – 1060 KiloPascal
Type
Storage Environment Temperature
Temperature Range
-40 – 66 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
10 – 95 Percent (%) Relative Humidity