FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 00763000332112 · Model: BB2K05R38 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00763000332112
Version / Model
BB2K05R38
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-11
Public Version
3
Public Version Date
2023-11-22
Public Version Status
Update
Public Device Record Key
cf1b9e07-12fb-4b20-b9d7-9b38057926d8
Distribution End Date
2023-11-01

Device Description

CUSTOM PACK BB2K05R38 MEMBRA

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass

GMDN Terms

Code Name
35441 Cardiopulmonary bypass system blood tubing set

Identifiers

Type ID
Primary 00763000332112

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K171308 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 50 Degrees Celsius