FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 00199150027644 · Model: BB12P94R1 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
NA
Primary DI
00199150027644
Version / Model
BB12P94R1
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-06-29
Public Version
2
Public Version Date
2026-03-27
Public Version Status
Update
Public Device Record Key
7ec35e3e-3a11-4e37-9ff6-06d31a21b90a
Distribution End Date
2026-03-20

Device Description

CUSTOM PACK BB12P94R1 IOM SUPPORT

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 00199150027644

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K171979 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 50 Degrees Celsius