FDA UDI In Commercial Distribution 🇺🇸 United States

BD PosiFlush

DI: 00382903065219 · Model: 306521 · BECTON, DICKINSON AND COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
3
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
BD PosiFlush
Primary DI
00382903065219
Version / Model
306521
Catalog Number
306521
Company Name
BECTON, DICKINSON AND COMPANY
Labeler DUNS
001292192
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
4
Public Version Date
2024-05-20
Public Version Status
Update
Public Device Record Key
6f4176b5-a7fe-4c96-b0ee-2ddb9140e2d6

Device Description

HEPARIN 10UL 3ML FILL IN 10ML SYRINGE

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FOZ Catheter,intravascular,therapeutic,short-term less than 30 days

GMDN Terms

Code Name
64786 Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial

Identifiers

Type ID
Package 50382903065214
Primary 00382903065219
Package 30382903065210

Premarket Submissions

Submission Number Supplement Number
K011967 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
20 – 25 Degrees Celsius