FDA UDI In Commercial Distribution 🇺🇸 United States

Omnifix®

DI: 04046955607808 · Model: 4617029-02 · B. BRAUN MEDICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Omnifix®
Primary DI
04046955607808
Version / Model
4617029-02
Catalog Number
4617029-02
Company Name
B. BRAUN MEDICAL INC.
Labeler DUNS
002397347
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2020-11-10
Public Version
6
Public Version Date
2024-01-25
Public Version Status
Update
Public Device Record Key
57fa61c6-8a1e-46d9-9c58-ce1d7eb3ad53

Device Description

OMNIFIX 2 ML LL LDS DISPLACEM. SPIKE 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
35904 Metered-delivery hypodermic syringe

Identifiers

Type ID
Package 04046955607815
Primary 04046955607808
Unit of Use 04046955607792

Customer Contacts

Device Sizes

Type Value Unit Text
Total Volume 2 Milliliter