FDA UDI Not in Commercial Distribution 🇺🇸 United States

Omnifix®

DI: 04046964723261 · Model: US4616502F-02 · B. BRAUN MEDICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
40

Basic Information

Brand Name
Omnifix®
Primary DI
04046964723261
Version / Model
US4616502F-02
Catalog Number
US4616502F-02
Company Name
B. BRAUN MEDICAL INC.
Labeler DUNS
002397347
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
40
Record Status
Published
Publish Date
2016-09-23
Public Version
5
Public Version Date
2020-03-03
Public Version Status
Update
Public Device Record Key
be6e1527-aa34-4a02-b53f-f8e05c19616f
Distribution End Date
2018-12-07

Device Description

OMNIFIX 50 ML US

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
FMF Syringe, piston

GMDN Terms

Code Name
47017 General-purpose syringe, single-use

Identifiers

Type ID
Primary 04046964723261
Unit of Use 04046964723254

Customer Contacts

Device Sizes

Type Value Unit Text
Total Volume 50.0 Milliliter