FDA UDI In Commercial Distribution 🇺🇸 United States

Unistik VacuFlip

DI: 00384707125014 · Model: BC 7125 · OWEN MUMFORD USA INCORPORATED
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Unistik VacuFlip
Primary DI
00384707125014
Version / Model
BC 7125
Company Name
OWEN MUMFORD USA INCORPORATED
Labeler DUNS
803401454
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2023-09-22
Public Version
1
Public Version Date
2023-10-02
Public Version Status
New
Public Device Record Key
c8037cc1-5632-44c7-8c1a-6127b8779568

Device Description

Unistik VacuFlip, 21G safety needle 1.25"

Device Characteristics

Single Use
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FMI Needle, Hypodermic, Single Lumen
JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

GMDN Terms

Code Name
58497 Blood collection set, invasive

Identifiers

Type ID
Package 00384707125038
Primary 00384707125014
Unit of Use 00384707125007

Premarket Submissions

Submission Number Supplement Number
K223854 000