FDA UDI In Commercial Distribution 🇺🇸 United States

Omnican®

DI: 04046955064335 · Model: 929G12S-02 · B. BRAUN MEDICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Omnican®
Primary DI
04046955064335
Version / Model
929G12S-02
Catalog Number
929G12S-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
2018-09-22
Public Version
4
Public Version Date
2021-08-30
Public Version Status
Update
Public Device Record Key
cc53212c-cc91-491d-b1c9-16d28fccaa6d

Device Description

OMNICAN FINE PEN NEEDLE 29GX12MM WCAP 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
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
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

GMDN Terms

Code Name
44127 Autoinjector needle

Identifiers

Type ID
Package 04046955064342
Primary 04046955064335
Unit of Use 04046955064328

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K173803 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Outer- cannula : 0.330 MM
Device Size Text, specify Length of cannula (inch) : 1/2"
Device Size Text, specify Length of cannula (metric) : 12.000 MM
Device Size Text, specify Gauge (cannula) : 29