FDA UDI In Commercial Distribution 🇺🇸 United States

Onyx 34

DI: 00836462005051 · Model: 105-7100-080 · Micro Therapeutics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Onyx 34
Primary DI
00836462005051
Version / Model
105-7100-080
Company Name
Micro Therapeutics, Inc.
Labeler DUNS
826110710
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-22
Public Version
5
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
913e5a83-1bf8-4fe8-8545-3f8b282fb2fb

Device Description

Liquid Embolic 105-7100-080 Onyx 34

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MFE Agent, injectable, embolic

GMDN Terms

Code Name
60939 Neurovascular embolization plug

Identifiers

Type ID
Primary 00836462005051

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P030004 008

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry;AVOID DIRECT SUNLIGHT
Type
Storage Environment Temperature
Temperature Range
-20 – 55 Degrees Celsius