FDA UDI Not in Commercial Distribution 🇺🇸 United States

Omnifix™

DI: 04046963451936 · Model: 4612042-02 · B. BRAUN MEDICAL INC.
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Omnifix™
Primary DI
04046963451936
Version / Model
4612042-02
Catalog Number
4612042-02
Company Name
B. BRAUN MEDICAL INC.
Labeler DUNS
002397347
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2016-09-23
Public Version
5
Public Version Date
2021-03-19
Public Version Status
Update
Public Device Record Key
aea6f38b-c374-4dc0-af08-d57121f51d52
Distribution End Date
2020-06-01

Device Description

20 mL LL 21 Ga. x 1-1/2 in.

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
Yes
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
FMI Needle, hypodermic, single lumen
FMF Syringe, piston

GMDN Terms

Code Name
47017 General-purpose syringe, single-use

Identifiers

Type ID
Package 04046963451929
Primary 04046963451936
Unit of Use 04046964332807

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Gauge (cannula) : 21
Total Volume 20.0 Milliliter