FDA UDI Not in Commercial Distribution 🇺🇸 United States

Omnifix™

DI: 04046963441999 · Model: 4610522-02 · B. BRAUN MEDICAL INC.
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Omnifix™
Primary DI
04046963441999
Version / Model
4610522-02
Catalog Number
4610522-02
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
6
Public Version Date
2021-03-19
Public Version Status
Update
Public Device Record Key
04330fb2-04d9-45a5-b10d-9d7c370bac8c
Distribution End Date
2020-04-04

Device Description

5 mL LL 21 Ga. x 1 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 04046963442309
Primary 04046963441999
Unit of Use 04046964332401

Customer Contacts

Device Sizes

Type Value Unit Text
Total Volume 5.0 Milliliter
Device Size Text, specify Gauge (cannula) : 21